Device for magnetic stimulation

TECHNICAL FIELD

The invention relates to devices and instruments for magnetic effect, which can be applied in medicine and veterinary medicine to perform magnetic physiotherapy or magnetic stimulating effects on the tissues and internal organs of a human being or an animal in order to eliminate pain syndromes, stimulate the processes of vital activity and regeneration, accelerate recovery of human and animal tissues after invasive effects and injuries.

PRIOR ART

Magnetic stimulation is one of the most promising methods of magnetic impact on the tissues and internal organs of a human being. Magnetic stimulation in various amplitude-frequency ranges has proven to be effective in prevention and treatment of central nervous system diseases, wounds and bone fractures healing, as well as sensory systems functional recovery.

Magnetic therapy is a non-invasive, safe and easy-to-use method for pain management, treatment of inflammation, injuries and other diseases and abnormalities. Magnetic fields cause orientation and concentration changes of biologically active macromolecules, thus affecting the kinetics of biochemical reactions and the speed of biophysical processes in the body. The field can affect macromolecules not only directly, but also through its influence on the environment of these molecules, including water with compounds dissolved in it, in particular, ions. The primary effect of fields on the body includes an orientation rearrangement of cell membranes, building the cell wall and forming the basis of intracellular structures. This affects both the permeability of the cells themselves and their organoids, and general biochemical processes in the body. Alternating magnetic field interacts with charged particles in the human body, such as ions and electrons, affecting their movement, for example, through ion channels, as well as contributing to generation of local electric fields (currents).

Thus, the magnetic fields impact body tissues by means of generated electric fields (currents). In the course of implementing actions on living systems submolecular, molecular and supramolecular structures are involved, resulting in changes at the cellular, system and organismic levels.

To assess the novelty of the claimed solution, we will consider a number of known technical means of similar purpose, characterized by a set of features similar to the claimed device.

Magnetic therapy device “Almag+” is known https://elamed.com/dlya-domashnego-primeneniya/produktsiya/almag-plus, which consists of an electronic unit, being a current oscillator, as well as four inductors in the form of applicators containing flat coils, and using magnetic field parameters in the frequency range from 4 Hz to 16 Hz. Type and parameters of the coils used, as well as the intensity of the impact are not disclosed.

Magnetic pulse therapy device “Ortomag” is known http://www.gzas.ru/products/4/prod1495.html, which contains a generator and 6 flat coils (inductors) attached to the human body, each of them generates pulsed magnetic field with about 6 Hz frequency, and an amplitude value of the magnetic field induction of at least 20 mT. Used coils type and parameters are not disclosed.

Patent EA 201500822 describes a device for local magnetic therapy, containing current source connected to an inductor, while the inductor contains magnetic field concentrator made in the form of a rod made of a magnetic conducting material, elongated in the direction of the target. The device is characterized by the fact that the inductor is made in the form of a set of two or more coils located along the axis of coils concentrator, made by bifilar winding.

There are known devices working according to darsonvalization and inductothermy methods and using high frequency alternating electromagnetic oscillations, refer to Physiotherapy. L. M. Klyachkin, M. N. Vinogradova, M. Medicine, 1995.

Besides, limited use of flat bifilar coils, called Tesla coils, is known in magnetic therapy. Tesla coils are used in radio engineering to neutralize self-induction (inductive resistance of the coil) in order to reduce current losses. Self-induction neutralization is possible at a certain frequency of cutoff current corresponding to the resonant frequency of “coil inductance—distributed design capacity” system. The resonant frequency of the system is determined by the coil design parameters—coil diameter, windings number of turns, and wire diameter.

According to patent RU No. 184786, there is device for treatment with the electric field, containing interconnected AC source and a therapeutic electrode, whereby a replaceable coil is used as the treatment electrode, in the form of capacity-coil connected to the signal duration control unit, the latter connected to the controller, the output of which is connected to the AC power source input. The inductor is a modification of Tesla coil and is made in two types—the capacity-coil in the form of a flat disk and the capacity-coil in the form of a toms. A disk capacity-coil may have several options: disk coil-bifilar, a disk coil-bifilar with cross-switching of turns of different wire diameters equidistant from the beginning and end of the coil, a disk coil—trifilar with contacts equidistant from the beginning and end of the spiral.

The device under patent RU No. 184786 has some design features similar to the claimed solution, so it is accepted as its prototype.

The description of the prototype indicates that the technical result of its usage is the increase of the therapeutic intervention effectiveness at the cellular level due to the increase of the electric field impact and the depth of its penetration. However, the possibility to achieve the claimed result using this device for electric field therapy, which is, namely, the generic concept of the device according to the patent, is practically excluded, since only the combination of electric and magnetic components has a penetrating effect, and it is much more difficult to stop the magnetic component than the electric one, i.e. its penetrating ability is much higher.

The disadvantage of known magnetic therapy devices is that the magnetic effect is poorly directed and is often accompanied by significant thermal effect, expressed in the heating of nearby tissues and organs surrounding the target area of magnetic stimulation, due to high-intensity magnetic field impact on them. Targeted stimulation of local areas with pathology in the body remains an actual problem. In addition, many of the known devices have large dimensions and/or multiple inductors, so that their usage is only possible within the walls of a medical facility. The entire volume of biological tissues in the projection of the generating electrode (inductor) is exposed to the influence of the created magnetic field—both pathological areas and tissues, and those that obviously do not require external intervention, i.e. healthy ones. Besides, in all cases, one or more parameters of such exposure (frequency, intensity of radiation, duration) do not correspond to known and proven ideas related to magnetic exposure safety.

SUMMARY OF THE INVENTION

The task of claimed invention is to create a device to perform targeted local magnetic stimulating and physiotherapeutic exposure, combining the effectiveness in a specific area of impact on cells, tissues and structures of a living organism, in particular, management of pain of various etiologies, and at the same time producing a minimal impact on the tissues and organs surrounding the exposed area, without causing a thermal effect in the course of application, as well as compact, simple and user friendly in line with the usual life routine.

The essence of the claimed technical solution is expressed in the following set of essential features.

According to the invention the device for magnetic impact on living organisms, containing the power source, the generator and the inductor connected to it, is characterized by the fact that the oscillator operates at the resonant frequency of the inductor, made in the form of flat bifilar coil with open windings connected to the oscillator as a load in the form of series-oscillating circuit, providing sinusoidal output current at the resonant frequency of the coil, while the bifilar coil is made in the form of a flat disk with the windings wires located at the dielectric substrate as two concentrically arranged spirals of two adjacent wires of different windings; at that the open-circuit terminal of one of the windings of the bifilar coil is located at the internal end of the specified winding in radial axis, and open-circuit terminal of the second winding of the inductor is located at the external end of the specified winding in radial axis, at that the opposite terminals of both windings of the coil are connected to respective terminals of the oscillator.

This combination of essential features of the claimed invention is sufficient to solve the technical problem, specified by the applicant, and to obtain the technical result provided by the invention.

In addition, the claimed technical decision is characterized by the presence of a number of additional optional features:

- the inductor can be structurally combined with the oscillator;
- the windings of the bifilar coil can be made as two identical conduplicated wires, located in the winding plane with tight junction of all wires to each other, providing total thickness of the winding equal to one wire diameter;
- the windings of the bifilar coil can be made as two identical conduplicated wires with the location of the winding wires perpendicular to the plane of the coil, providing total thickness of the winding equal to two wire diameters;
- the oscillator can be made in the form of self-excited oscillator of sinusoidal or square oscillations with a coil in the Positive Current Feedback Loop (PCFL);
- the oscillator can be made in the form of self-excited oscillator of sinusoidal oscillations with a coil in the PCFL circuit with amplitude modulation or manipulation;
- the oscillator can be equipped with a Negative Voltage Feedback (NVF) circuit with the ability to regulate the output voltage and, respectively, the output current and the magnetic field intensity, generated by the inductor by changing the NVF depth;
- the oscillator can be made as voltage-controlled oscillator with Automatic Frequency Control (AFC);
- the resonant frequency of the bifilar coil, as series-oscillating circuit, and the operational frequency of the oscillator is selected in the range of 250-380 kHz.

The claimed combination of essential and optional features ensures the achievement of technical result, residing in the fact that the inductor of device for magnetic action provides directed magnetic effect on human tissues and organs with the formation of inhomogeneous magnetic field of principally conical shape, providing maximum intensity of such effect, i.e., the maximum of the magnetic field induction located at the top of the specified cone. Device execution in a compact, ergonomic form increases the level of positive emotions of users in the course of its application, contributes to patients' commitment to treatment, i.e to compliance, providing higher indicators of the treatment process efficiency.

BRIEF DESCRIPTION OF THE DRAWINGS

The essence of the invention is explained with the drawings, where

FIG. 1 provides a design view of the inductor, made in the form of a flat bifilar coil,

FIG. 2—electrical diagram of the windings of the flat bifilar coil,

FIG. 3—the connection diagram of the power supply, oscillator and inductor,

FIG. 4—general view of the oscillator and the inductor, made, respectively, in the form of a round device and a flat disk,

FIG. 5—diagram, representing the shape of generated magnetic field intensity,

FIG. 6—diagram of the bifilar coil magnetic field intensity distribution along its vertical and horizontal axis,

FIG. 7—functional diagram of the oscillator in the form of self-excited oscillator with a bifilar coil in the PCFL circuit;

FIG. 8—stress distribution diagrams at test points T1, T2 of self-excited oscillator with the PCFL;

FIG. 9—functional diagram of the oscillator in the form of self-excited oscillator with AFC,

FIG. 10—stress distribution diagrams at the test points T1, T2 and T3 in the position S1-1 of S1 switch of the generator with a AFC,

FIG. 11—stress distribution diagrams at test points T1, T2 and T3 in the position S1-2 of switch S1 of the generator with a AFC.

Items and letters marked at the drawings: 1—the first (closed-circuit) terminal of the first winding; 2—the second (open-circuit) terminal of the first winding; 3—the third (open-circuit) terminal of the second winding; 4—the fourth (closed-circuit) terminal of the second winding; 5—L1—inductor's bifilar coil; 6—substrate; 7—the first winding of the bifilar coil; 8—the second winding of the bifilar coil; 9—oscillator; 10—power supply; 11—inductor housing; 12—oscillator housing; 13—connecting cable for inductor connection to the oscillator; 14—bifilar coil axis; 15—oscillator node; Di—internal diameter of the bifilar coil; Do—outer diameter of the bifilar coil; K1, K2—generator terminals; A1—generator node (self-excited oscillator); DA1—amplifying stage covered with feedback communication; R1, R2, R3—resistors; +IN, −IN—amplifying stage input terminals; OUT—amplifying stage output terminals; AFC—automatic frequency control; LPF—low pass filter; S1—AFC output voltage form switch; S1-1, S1-2—S1 switch positions; PD—phase detector; VCO—voltage controlled oscillator; T1—self-excited oscillator output voltage test point; T2—coil output current test point; T3—AFC output voltage test point, U1—oscillator/self-excited oscillator output voltage, U2—the voltage at the current transducer, U3—AFC output voltage.

DETAILED DESCRIPTION OF THE INVENTION

Flat bifilar coil 5 of the inductor is formed by two identical conductors, also called winding wires, wound in two wires in a single layer in the same plane, in the form of a flat spiral from the inner diameter Di to the outer diameter Do, with firm adherence of adjacent conductors and adjacent winding turns to each other without gaps between them. Adjacent conductors form, respectively, the first winding 7 and the second winding 8 of the flat bifilar coil 5. Windings 7, 8 can be wound with a single-core or multi-core winding wire with enamel or lacquer insulation. The thickness of the bifilar coil 5 is equal, respectively, to the thickness of one winding wire. Windings 7, 8 of the bifilar coil 5 can be made as helical winding in one plane with two identical wires put together with vertical arrangement of the winding wires, i.e. perpendicular to the plane of its winding, with “two wires—to two wires” connection to each other, while ensuring the total thickness of the winding equal to two diameters of the winding wire. Bifilar coil 5 can also be made as two flat windings with the thickness of one wire, located with their planes opposite and parallel to each other on different sides of the substrate, i.e. with the separation of both windings of the coil with the substrate. The first winding 7 of coil 5 has the first terminal 1 and the second terminal 2. The second winding 8 of coil 5 has, respectively, the third terminal 3 and the fourth terminal 4. The second and the third terminals 2, 3 of coil 5 are open-circuit. Open-circuit terminal 2 of the first winding 7 of coil 5 is located at the internal end of the specified winding in the radial direction of the coil and open-circuit terminal 3 of the second winding 8 of coil 5 is located at the outer end of the specified winding in the radial direction of the coil. It is possible to have reverse location of open-circuit terminals of coil 5, when the open-circuit terminal 2 of the first winding 7 of coil 5 is located at the outer end of the specified winding in the radial direction of the coil, and the open-circuit terminal 3 of the second winding 8 of coil 5 is located at the inside end of the specified winding in the radial direction of the coil. The first (closed-circuit) terminal 1 of the first winding 7, located at the outer end of the specified winding in the radial direction of coil 5, and the fourth (closed-circuit) terminal 4 of the second winding 8, located at the inner end of the specified winding in the radial direction of coil 5, are normally connected to the signal source or self-excited oscillator circuit with two-wire cable. Windings 7, 8 of bifilar coil 5 are located at flat substrate 6 in the form of a round plate made of a dielectric material, such as, for instance, plastic or wood. At that, terminal 1 of the first winding 7 and terminal 4 of the second winding 8 are led outside the substrate 6 for their connection with terminals K1, K2 of the oscillator 9, and the opposite open-circuit terminals 2 and 3 of the specified windings are embedded in the substrate 6 and not projected outside the coil.

In electrical equivalent, coil 5 is series-oscillating circuit. In the embodiment of invention shown in FIG. 3, 4, the coil is structurally separated from the oscillator, the first terminal 1 and the fourth terminal 4 of coil 5 are connected to the voltage outputs K1 and K2 of the oscillator 9. Oscillator 9 is connected to DC power source 10 which is a rechargeable battery.

Depending on the embodiment of the device for magnetic effect, the oscillator and the coil can be combined in a common housing; the generator can be powered from the AC network via an AC or DC adapter.

On the inductor housing (or on the housing of device containing the inductor) there may be provided attachments to the user's clothing in the area of desired magnetic stimulating or therapeutic effect to avoid the need to hold the device in the course of operation.

Coil 5 inner diameter Di principally determines the diameter of the toroid formed in the top of the cone generated by coil 5 of the magnetic field inductor due to the interference of separate magnetic fields generated by each turn of winding of bifilar coil 5.

Oscillator 9 schematically can be a generator with manual resonance frequency tuning or self-excited oscillator with PCFL or voltage controlled oscillator with a AFC, and the inductor is series-oscillating circuit being the load of the specified generator, inducing magnetic oscillations.

The claimed device works as follows.

Oscillator 9 supplies voltage to coil 5 with at the resonance frequency of the coil, the self-excited oscillator automatically operates at the resonance frequency of the coil. Due to field density multiplication cone-shaped form of the magnetic field is achieved with the maximum intensity at the top of the cone due to turns density reduction from the center to the edge of coil 5. At that, the height of the cone above coil 5 surface depends on the coil diameter and the strength of induction current through the coil.

Table 1 shows the values of the magnetic field induction measured along the mutually perpendicular directions N, W, E, S in the plane of coil 5.

TABLE 1

Displacement from

the center, cm
N
S
W
E

0
4
4
4
4

1
4
4
4
3.6

1.5
3.8
3.6
3.8
3

2
3
3
3.4
1

3
2
2
2
1

4
1
1
1
1

Table 2 shows the magnetic field induction values measured along the mutually perpendicular directions N, W, E, S at 5 cm distance from the coil plane.

TABLE 2

Displacement from

the center, cm
N
S
W
E

0
5.4
5.4
5.4
5.4

1
5
5.6
5
5.4

2
4.6
5.4
4.6
5

3
4
5.2
4
4.6

4
3.4
4.8
3.4
4

5
1
4.2
2
3

6
1
3.6
2
2.8

7
1
3
2
2

8
1
1
1
2

9
1
1
1
1

The shape of the distribution of the magnetic field strength of coil 5 has the characteristic frusto-conical shape and in projection on the base plane reflects the features of its winding.

The resonance frequency of the series-oscillating circuit implemented in the claimed device in the form of bifilar coil 5 is determined by coil 5 parameters, in particular its geometric dimensions, number of turns of its windings, internal and external diameter of the windings, as well as the diameter (cross section) and length of the winding wire. The length of the wire of selected section is determined by the size of the coil, the winding method, and the number of turns.

Coils of different sizes can cause comparable therapeutic effect, and the most significant in terms of achieving stimulating and therapeutic effect is the directional form of obtained magnetic field, as well as its frequency and intensity value. In this case, most of the above parameters are determined by the geometric parameters of the inductor coil 5. Excitation of oscillations, and, respectively, generation of a magnetic field with the inductor, occurs at the resonance frequency of coil 5 of the inductor. Coil current oscillations have sinusoidal shape. In order to stabilize oscillations and to reduce nonlinear distortions, the circuit can additionally be covered with the NVF circuit.

Thus, the oscillating circuit, executed as bifilar coil with open-circuit turns, acts both as frequency-setting element and at the same time as an inductor loading the oscillator.

The resonance frequency of the oscillation circuit formed by the inductor coil is 250-380 kHz, preferably 280-350 kHz. The specified frequency range is the frequency range determined on the basis of performed research as the most effective and safe range of operating frequencies of generated magnetic impact in order to ensure the best and stable stimulating and therapeutic effect.

Due to the effect of oscillating magnetic field, in the specified range of oscillation circuit resonance frequencies, the most represented and stable magnetic stimulating and therapeutic effect is provided, consisting in elimination of pain syndromes, stimulation of life processes and regeneration, accelerating the recovery of human and animal tissues after invasive effects and injuries.

The oscillator is designed with a possibility to regulate the output voltage and, respectively, the values of output current and intensity of magnetic field, generated by the inductor. The oscillator can also be provided with means for regulating duration, number of cycles or frequency of repetition of generated magnetic impact, as well as its modulation and manipulation with low-frequency signals.

Impact intensity can be pre-set by the oscillator parameters and set in the range most effective and safe for the user, ranging from 80 μT to 200 μT, and, in this case, only regulation of impact duration can be provided. Executed experiments have shown that magnetic impact generated by the inductor of the present invention with the magnetic field intensity in the range from 80 μT to 200 μT provides achievement of stable therapeutic effect, while the intensity of the magnetic field in the plane of the inductor remains comparable with the value of the Earth magnetic background, comprising about 50-60 μT, which provides a minimal impact on human tissues and organs surrounding the impact area, and thus also excludes the occurrence of undesirable thermal effect.

Oscillator execution as self-excited oscillator simplifies the implementation of the claimed device and provides automatic excitation of oscillations in the inductor coil at its resonance frequency.

Magnetic field shape, provided by the claimed device, enables to perform directed magnetic stimulating effect on human tissues and organs located directly under the application site of the inductor at up to 6 cm depth from the surface of the body. Exposure to such magnetic field by applying the specified inductor to areas of the body located above pathogenic areas, in particular over painful organs within 15-30 minutes, provides directed “local” effect on the areas of the body exposed to magnetic impact with pain management for a long period of time. At that, the shape of the magnetic field of the claimed device allows to actually eliminate the main side effect of the magnetic field in the course of application of known state-of-the-art devices on healthy tissues surrounding the target area, in particular, magnetic stimulation, which can sometimes cause development of new pathologies or escalation of existing ones. This disadvantage is eliminated due to application of “focused” magnetic field with the maximum of its intensity, concentrated at the top of the “magnetic cone”, i.e. limited to a small area of “directed” influence.

A series of experiments with the claimed device proved that the therapeutic effect of eliminating or reducing pain syndromes of various etiologies is achieved primarily due to the properties of inhomogeneous and directed magnetic field applied. 250-380 kHz range of resonance frequencies, determined by the results of experiments, as well as 80-200 μT range of magnetic field intensity, allow obtaining even more significant magnetic stimulating and therapeutic, in particular, pain relieving effect, without the danger of local heating of adjacent tissues.

Example 1. Testing on the Proliferation Model

The study was conducted at the “Scientific center of cytogenetic testing” LLC in January, 2019.

The device was tested at different device capacities, namely, at 50% (90-100 μT) and 100% (180-200 μT), and at different distances (0 cm and 4 cm) in order to determine the effect of the device on the proliferation of cells of the CHO-K1 line.

The cells were plated at the rate of 200 μl of medium per well of a 96-well plate. The medium comprised 9 parts of the DMEM (or EMEM) substrate with addition of 1 part of the embryonic veal blood serum. Cells suspension with 2×104 cells/ml seeding concentration was prepared. To do this, culture flasks (25 cm²or 75 cm²in area) with formed cells monolayer (2-4 days cell culture with normal cell morphology) were selected; the cell monolayer was dispersed: 2-5 ml of substrate was added to the culture flask; the contents of the flask were mixed with a 10 ml pipette; a sample was taken and the cell suspension was transferred to Eppendorf type microcentrifuge tube. Then the concentration of cells was calculated in Goryaev chamber. Cell suspension was diluted with substrate to required final cell concentration. 0.2 ml cell suspension of was added to the required number of wells (based on the number of samples studied) in two 96-well plates. The plates with cells were incubated for three days at 37±0.5° C. in an atmosphere with 5±0.7% CO2 content at different shelves of the incubator. At that, the control plate was placed on a shelf, and the test plates were placed strictly in the middle directly opposite operating magnetic impact device at 4 cm distance from the surface, using plastic tubs or tripods as lifting facility. This arrangement was repeated with 50% and 100% capacity of activated device. Upon completion of the incubation period, the plates were removed from the incubator, the substrate was completely removed from the wells, 100 μl of trypsin-versene solution (1:9) was poured and left for 10-15 minutes to completely detach the cells from the substrate. The content of the well was mixed with a dispenser and 10 μl were added to Goryaev chamber. The cells were counted cornerwise in five large squares. The obtained number was multiplied by 1.25 and 104 co-efficient, and thus determined the number of cells in ml. The procedure was repeated for each well. Then the proliferation index (PI) was calculated as the ratio of cells concentration after three days of cultivation to the seeding concentration. PI for control and test were calculated separately. Then the Impact index was calculated as the ratio of test and control options, using the following formula: ((test IP/control IP)*100−100).

Test results proved that proliferation increases by 7-40%, depending on exposure power and the distance from the plate to the device.

Example 2. Testing on the Wounds Model

Testing to determine the specific activity of the device on the wound model (“wound healing assay”). Wound model in vitro is widely used technique for evaluation of cells mobility and migration rate. In the course of experimental wound healing different types of cells react in a similar way: the cells polarize, form protrusions towards the wound, and migrate (Yarrow et al., 2004). The study was conducted at the “Scientific center of cytogenetic testing” LLC in compliance with the standard protocol for this procedure.

The study demonstrated the increase of “wound” healing rate in case of application of the device according to the invention on cell culture by 12%.

Example 3. Treatment of Hemorrhoids

In February 2019, the device was tested in St. Petersburg at private clinics on men with symptoms of hemorrhoids of 3-4 degrees (20 people aged from 30 to 60 years). The tests were aimed at studying the effect of relieving pain and other senses of discomfort. Magnetic therapy sessions were conducted within 14 days for 30 minutes each day at a radiation intensity of 180-200 μT (100% of the device's capacity). This intensity of the magnetic field eliminates the occurrence of undesirable side effects, in particular, the thermal effect. The magnetic disk was applied by the patient to the area of maximum pain. Selected group included both patients using additional medications and patients not receiving pharmaceutical treatment. All patients, participating in the study, described the disappearance of characteristic pain on the day 2-3 after commencement of the study; in some cases, arrest of hemorrhage was noted in acute forms of the disease, and tumorous and edematic phenomena reduction upon completion of therapy in 14 days. In each case, the proctologist conducted an objective examination before and after magnetic therapy sessions, which confirmed the subjective feeling of remission.

Example 4. Treatment of Prostatitis

In February, 2019 the device was tested on men with prostatitis symptoms at private clinics in Saint Petersburg. 20 men aged from 40 to 60 years participated in the study. The magnetic disk was applied by the patient to the area of maximum pain. Selected group included both patients using additional medications and patients not receiving pharmaceutical treatment. As a result, a positive effect of pain reduction subjective perception was observed within 10-14 days according to the described method. Objective confirmation of the test result was based on laboratory analysis of lymphocytes number in special effusion, which demonstrated lymphocytes number decrease by 12-15% as a result of magnetic device application. It is assumed that the impact efficiency can be significantly increased in case of implementation of direct access to the hotbed of disease by means of changing the design parameters of the device, resulting in increase of active magnetic field intensity in the pathology zone.

Example 5. Menstrual Pain Syndrome

The study was also conducted in February, 2019 at private clinics. 50 women aged from 18 to 24 years with menstrual pain syndrome voluntarily participated in the study. Magnetic therapy sessions were conducted within 2-4 days for 30 minutes each day at 180-200 μT radiation intensity (100% of the device capacity). The study revealed positive dynamics based on subjective feelings of more than 60% of participants already on the second day of device application. To objectify the assessment, it is required to clarify the diagnosis, for example, endomitriosis or polycystic ovary, etc. In each of examples 3-5 none of the patients had any adverse events that could be associated with device application. Reexamination of patients in 2-3 months demonstrated that the aftereffect duration upon completion of the magnetic therapy session is 30-45 days in 54% of the subjects.

Thus, the claimed device allows to exercise targeted magnetic stimulating effect expressly on pathogenic areas and organs located at 3-6 cm depth from the skin surface, while practically not affecting the tissues located on and near the skin surface, to which the inductor (applicator) coil is attached. The shape of the magnetic field of the inductor, made in the form of the bifilar coil, provides an impact on specified areas in order to localize pain of various etiologies.

Main characteristics of the claimed device:

- inductor output current effective value 0.01-2.00 A;
- oscillator output voltage effective value 1.5-10V;
- induced magnetic field intensity—80-200 μT.

Device design features and portability allow to “deliver” the magnetic impact signal to the target area of the human body locally, as well as, if required, affect multiple foci and central processes. Thus, the claimed device comprises a compact device for general medical purpose magnetic stimulation, suitable for application in clinical or home conditions for treatment of menstrual syndrome, hemorrhoids, joint diseases, as well as for relieving pain of various etiologies and for healing injuries and stimulating cell proliferation.

Device for magnetic stimulation

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