Patent Grant
6949067
1. Field of Invention
The present invention relates generally to a device and method to increase female sexual stimulation and, more specifically, to a female stimulation device and method which provides vascular engorgement.
2. Description of the Related Art
Clitoral vascular engorgement plays an important role in female sexual arousal and satisfaction. Sexual arousal results in smooth muscle relaxation and arterial vasodilation within the clitoris. The resultant increase in blood flow leads to tumescence of the glans clitoris and increased sexual arousal. A variety of diseases, such as arteriosclerosis and diabetes, may cause clitoral erectile insufficiency and reduced clitoral arterial flow. This, in turn, may lead to difficulty or inability to achieve clitoral tumescence, especially in women who suffer from female sexual arousal disorder (FSAD). FSAD may be expressed as a lack of either subjective excitement, genital lubrication or orgasmic function.
The most effective method of increasing clitoral engorgement, especially in women suffering from FSAD, is through use of suction. A partial vacuum placed over the clitoris creates negative pressure in the organ which promotes clitoral arterial inflow and venus congestion and results in increased vascular engorgement and sexual arousal. One device for stimulating female sexual response that is designed to be applied in the clitoral region is described in U.S. Pat. No. 6,733,438, which is incorporated herein by reference in its entirety. It consists of a vacuum-producing, partially deformable device of unitary construction having a distal tip portion, a flange and intermediate side walls which, when placed over the clitoris of the user, stimulates blood flow and sexual response. The intermediate side walls are outwardly convex so as to retain its shape rather than collapse when vacuum is applied. The side walls may be reinforced with internal or external arches. The arched geometry prevents side wall collapse and clitoral compression with injury.
In accordance with one or more embodiments, the present invention can provide a female stimulation device. The device includes a body having a tip portion, a flange, and an intermediate side wall portion. The intermediate side wall portion extending from the tip portion to the flange. The device also includes means for controlling vacuum produced by the device when applied to a user.
In accordance with one or more embodiments, the present invention can also provide a method for facilitating female stimulation. The method includes providing a device comprising a tip portion, a flange, and an intermediate side wall portion extending outwardly from the tip portion to the flange. The flange is sized and shaped to encompass the female clitoris. The intermediate side wall portion is outwardly convex and defines a vacuum reservoir lower chamber. The tip portion is deformable and defines a vacuum producing upper chamber that produces vacuum levels of between about 40 and about 190 mmHg in the lower chamber. The method further includes providing instruction to apply the device to promote clitoral blood flow without causing injury to underlying tissue.
In accordance with one or more embodiments, the present invention can also provide a method for enhancing female stimulation. The method includes providing a female stimulation device comprising a tip portion, a flange, and an intermediate side wall portion extending from the tip portion to the flange and defining an interior vacuum chamber. The tip portion is compressed to reduce an air column formed within the interior vacuum chamber. The device is placed over the female clitoris such that the flange is placed into contact with anterior vaginal vault tissue. The tip portion is released to produce vacuum levels of between about 40 and about 190 mmHg in the interior vacuum chamber. The vacuum causes clitoral engorgement and maintains engagement of the device with the anterior vaginal vault tissue. The device may be removed after a predetermined period of time. The method may be repeated periodically to condition and treat genital tissues.
The accompanying drawings are not intended to be drawn to scale. In the drawings, each identical or nearly identical component that is illustrated in various figures is represented by a like numeral. For purposes of clarity, not every component may be labeled in every drawing. In the drawings:
This invention is not limited in its application to the details of construction and the arrangement of components set forth in the following description or illustrated in the drawings. The invention is capable of other embodiments and of being practiced or of being carried out in various ways. Also, the phraseology and terminology used herein is for the purpose of description and should not be regarded as limiting. The use of “including,” “comprising,” “having,” “containing,” “involving,” and variations thereof herein, is meant to encompass the items listed thereafter and equivalents thereof as well as additional items.
In accordance with one or more embodiments, a device for stimulating the clitoris of a female includes a resilient and at least partially deformable device body having an enclosed tip portion, a flange, and an intermediate side wall portion. The side wall portion may extend outwardly from the tip portion to the flange. The device body is sized to encompass the clitoris of the user and is of unitary construction. In use, the device body is placed over the clitoris of the user and the tip portion is deformed, causing a vacuum environment to be formed in an interior chamber formed by the device body. The vacuum environment maintains the device in reliable sealed engagement around the clitoris. A biocompatible lubricant, adhesive, or pharmacologically active material such as vasoactive agent, may be applied to the flange in order to enhance the vacuum seal and to further increase clitoral blood flow. The amount of lubricant or pharmacologically active material should be on the order of 3 mm thickness or less to avoid device slippage.
With this arrangement, a small, simple, and effective female clitoral stimulation device provides suction to the clitoris, thereby stimulating vascular engorgement and sexual arousal. Advantageously, the device does not require an external vacuum source or associated tubing or connections. The device is simple to use, permitting the user to perform her daily activities while wearing it in an undetectable and discreet fashion.
In some embodiments the intermediate side wall portion has an outwardly convex shape. With this geometry, the intermediate side wall portion is substantially non-deformable in response to deformation of the tip portion. In other words, the vacuum producing tip portion is deformable while the outwardly convex geometry of the intermediate side wall permits the lower chamber to retain its shape, serving as a soft, yet functionally non-deformable, vacuum reservoir. With this arrangement, the device may be of unitary construction, manufactured from a single, soft, deformable material, yet possess both deformable and non-deformable portions. Furthermore, the soft, deformable material comprising the functionally non-deformable lower chamber will form a substantially fixed volume lower vacuum chamber over the clitoris, thereby preventing side wall abutment with associated tissue compression to genital tissue. The soft flange will prevent pressure necrosis of genital tissue when compared to rigid, non-deformable materials.
In some embodiments, the device may be made disposable by constructing it from low-tear strength materials. The low-tear strength materials permit the device to easily tear apart after one or more applications. To further increase the disposability of the low-tear strength material, one or more slits can be made in the flange. In another embodiment, the device can be made disposable by including a biodegradable plug in the tip portion which would degrade upon contact with the moist vaginal tissue. Once dissolved, an open channel would connect the device's inner vacuum chamber to the outside, therefore destroying the vacuum-producing potential for the device. In another embodiment, a patch of material can be attached over a hole in the wall of the device. Upon multiple uses, the patch will tear away. In another embodiment, a portion of a wall of the device is constructed extremely thin so as to rupture upon multiple uses. Disposability enhances safety by avoiding infection or contamination.
In some embodiments a method for increasing female sexual stimulation includes placing on the clitoris of the user a device body having a tip portion, a flange and an intermediate side wall portion extending outwardly from the tip portion to the flange so that the device body encompasses the clitoris. The method further includes deforming the tip portion so as to create a vacuum chamber within the device body. The intermediate side wall portion is substantially non-deformable in response to deformation of the tip portion. In the preferred embodiment, this is achieved by providing the intermediate side wall portions with an outwardly convex shape. With this arrangement, a fixed volume lower vacuum chamber is formed over the clitoris of the user in a simple manner that prevents pinching or compression of the clitoris. Furthermore, with this arrangement, the device may be of unitary construction, manufactured from a single, soft, compressible material, yet possess both deformable and non-deformable portions. The soft, yet functionally non-deformable, lower chamber and flange will further minimize tissue injury from compression or pressure necrosis.
Referring now to
The tip portion 16 has a substantially circular shape with vertical walls 17 and a curved outer end wall 19 which serves as a gripping portion to facilitate application and removal of the device in the manner described below. In an alternate embodiment, the outer end wall 19 of the tip portion 16 is flat. The interior of the tip portion 16 defines the upper vacuum chamber 18a. The tip portion 16 is at least partially deformable, or compressible, in order to produce a partial vacuum within the interior vacuum chamber 18 sufficient to seal the device 10 to the user's body by the differential in air pressure between the air within the vacuum chamber 18 and the atmospheric air pressure.
The intermediate side wall portion 22 extends outwardly from the bottom of the tip portion 16 to the flange 26. The interior of the intermediate side wall portion 22 forms the lower vacuum chamber 18b. The intermediate side wall portion 22 is designed so as to avoid compression of the clitoris. In the illustrative embodiment, the intermediate side wall portion is substantially non-deformable and maintains its shape when vacuum is applied by compression of the tip portion (as shown in
As noted above and illustrated in
The material 34, in the form of an adhesive, lubricant, and/or vasoactive substance, may be pre-coated onto only a portion or onto the entire body-contacting surface 29. In another embodiment, the lubricant or vasoactive substance may be stored within the tip portion 16 and spread onto the body-contacting surface 29 of the flange 26 when the user squeezes the vertical walls of the tip 17. In yet another embodiment, material 34 may be stored within intermediate side walls 24 for contact with tissue 39. If a lubricant or vasoactive substance is used, the amount disposed on the body-contacting surface 29 should be less than about 3 mm thickness since clinical studies have demonstrated that excessive amounts will over-lubricate the genital area and may subsequently cause device slippage. The material 34, in the form of an adhesive, lubricant, and/or vasoactive substance, may be covered by a thin layer of another material or coating (not shown). This material or coating may be used in packaging or application, to prevent material 34 from dissipating, migrating or drying. This material or coating layer would be removed prior to application. In one embodiment, the material or coating covers only body-contacting surface 29 of flange 26. In yet another embodiment, the material or coating may envelop flange sides 28, the non-body-contacting flange surface 27, or other portions of device 10. Furthermore, the adhesive, lubricant, and/or vasoactive substance may have a fragrant odor and/or pleasant taste so as to increase the arousal of the user or her partner.
Typically, device 10 is constructed of any resilient material that is at least partially deformable. The material should be suitable for application to the human body in the manner described. Such materials include silicone, thermoplastic elastomers, urethanes, or rubber materials. One particularly effective material for use in constructing device 10 has been found to be silicone rubber. Preferably, 30–60-durometer silicone rubber is effective. Most preferably, 40-durometer silicone rubber has been shown to be effective. It will be appreciated that although intermediate side walls 24 are comprised of a resilient, deformable material, the side walls are made substantially non-deformable in response to deformation of tip portion 16 by their geometry, which is outwardly convex in one embodiment. With this arrangement, the device may be of unitary construction and manufactured from a single, soft, deformable material, yet possess both deformable and non-deformable portions. In other words, the lower chamber may be formed from a soft material, yet be functionally non-deformable when vacuum is applied. Furthermore, the resilient, deformable material is generally soft in contacting area tissue. Therefore, the lower chamber and flange will minimize pressure necrosis and any potential damage to genital tissue when compared to rigid, non-deformable materials. As will be further appreciated, other manners of rendering the side walls substantially non-deformable in response to deformation of the tip portion are possible including, but not limited to, material selection, geometry, dimensions and reinforcing features.
In general, device dimensions are dictated by the typical female anatomy so as to comfortably fit over the clitoris within the anterior vaginal vestibule. In the preferred embodiment, the outer radii extending from the center of device 10 to the ends of intermediate side wall portion 22 may vary between about 0.50 cm and about 1.75 cm. The radii of tip portion 16 will vary in proportion to the dimensions stated above, but generally will be between about 0.25 cm and about 0.75 cm, respectively. Preferably, body-contacting surface 29 of flange 26 contacts vaginal tissue adjacent to the outer perimeter of the clitoris. With this arrangement, the efficacy of the device is enhanced by providing a focused vacuum area. The height of device 10 can also vary, but should comfortably fit within the anterior vaginal vestibule without excessive protrusion while also being capable of being accessible for handling. In the preferred embodiment, the height of device 10 is between about 1.5 cm and about 3.0 cm; more preferably, the height of device 10 is between about 2.0 cm and about 2.5 cm; most preferably, the height of device 10 is approximately 2.0 cm. It will be appreciated, however, that the exact dimensions and shape of device 10 can vary without departing from the spirit of the invention.
The vacuum by the device can be controlled by the user. The amount of compression of tip portion 16 of device 10 regulates the amount of negative pressure within internal vacuum chamber 18. If the user compresses tip portion 16 more vigorously, the negative pressure or vacuum increases. In the preferred embodiment, as clinical studies have demonstrated, negative pressures should enhance clitoral blood flow without causing clitoral injury. The studies have demonstrated that to achieve enhanced clitoral blood flow without causing clitoral injury, device 10 should produce a range of negative pressure between about 40 and about 190 mmHg. If negative pressures exceed about 190 mmHg, excessive suction may place users at risk and may result in bleeding, discomfort and tissue injury. Alternatively, negative pressures below about 40 mmHg will result in inadequate stimulation of blood flow to the clitoris, or in failure of the device to self-adhere to the genital area. Device 10, therefore, can be calibrated for its size, shape, and materials of construction to allow for a range of vacuum pressure of between about 40 mmHg and about 190 mmHg.
As noted device 10 may include structures to allow the user to select the most appropriate vacuum level for their need. The various structures may allow users to control the vacuum produced by the device when applied, rather than by the amount of compression of the tip portion 16 by the user. As noted above, based upon clinical studies, a preferred range of the vacuum produced by device 10 can be controlled between about 40 mmHg and about 190 mmHg. Alternatively, a variety of devices may be constructed such that each may have a capability to produce a range of vacuum pressure between about 40 mmHg and about 190 mmHg.
One embodiment of device 10 including structures that may allow users to control the vacuum produced when the device is applied is illustrated in
Referring to
Referring to
In an alternative embodiment, shown in
An alternative approach to limiting the compression of tip portion 16 and, therefore, the resulting negative pressure produced by the device is illustrated in
Another embodiment of device, shown in
The vacuum produced by the device may also be controlled by providing tip portion 16 and intermediate side wall portion 22 with walls of different thicknesses. Despite use of a resilient, deformable material, variation in wall thickness can change compression of tip portion and the resultant vacuum as shown in
Referring to
The device 10 can be made disposable or for limited reuse for safety by avoiding infection or contamination from excessive use or misuse. The device may be constructed from a low-tear strength material such as silicone, thermoplastic elastomers, urethane, and rubbers. The low-tear strength materials permit device 10 to easily tear apart after one to several applications. Referring to
Referring also to
The deformation of tip portion 16 reduces the air volume within the entire interior vacuum chamber 18 and produces a partial vacuum. The force created by the differential pressure between the outside atmosphere pressure and the pressure within the interior vacuum chamber will attempt to force intermediate side walls 24 inward toward the center of the vacuum chamber. If intermediate side walls 24 were deformable (e.g., flat or concave inward), sufficient vacuum applied to interior vacuum chamber 18 would cause intermediate side walls 24 to collapse inward toward or into an abutting relationship. In this case, the normally distensible clitoris 39 would be drawn into the compromised interior vacuum chamber 18 and compressed by the abutting intermediate side walls 24. Clitoral tissue could become entrapped and pinched by these abutting side walls 24. In the preferred embodiment, side walls 24 are shaped outwardly convex, like an arch, preventing inward movement of intermediate side walls 24 and thereby preventing clitoral entrapment and/or compression.
More precisely, the outwardly convex geometry of intermediate side walls 24 creates two functional chambers 18a and 18b which resemble a “bell.” The lower vacuum chamber 18b, formed by the outwardly convex intermediate walls, serves as a substantially non-deformable, constant volume vacuum reservoir, while upper vacuum chamber 18a, formed by the tip portion, serves to create the vacuum due to its side wall deformation. In this fashion, lower vacuum chamber 18b evenly distributes suction to the clitoral tissue without compressing, obstructing or pinching clitoral tissue. Stated differently, the outwardly convex wall geometry allows the device to be of unitary construction and manufactured from a single, soft, deformable material. The lower vacuum chamber 18b may be composed of a soft, deformable material, yet be functionally non-deformable when vacuum is applied. Furthermore, the soft deformable material composing the non-deformable lower chamber and flange will minimize pressure necrosis to genital tissues when compared to rigid non-deformable materials, thus further preventing tissue damage.
As noted above, the user can alter the amount of vacuum in the interior vacuum chamber 18 by varying the degree of compression of the tip portion and thus the amount of air that is displaced. The greater the amount of manual compression to the tip portion, the greater the amount of displaced air and subsequent vacuum. In this manner, the user can advantageously regulate the amount of clitoral suction in order to generate a physiological response, rather than rely upon predetermined vacuum from an external vacuum source. The amount of vacuum necessary to stimulate female sexual arousal may vary depending upon the user and her pre-excitatory state but is preferable between about 40 mmHg and about 190 mmHg. Clinical testing has demonstrated that this negative pressure range maximizes clitoral blood flow without causing discomfort, bleeding and tissue injury.
To achieve an optimal response, clinical testing has shown that the device should initially be utilized for a period of time to condition the genital tissues also known as a “conditioning period.” Users should apply the device for a specified period of time; up to as long as several weeks; preferably one to four weeks. The device should be applied on a daily basis for a predetermined period; for as long as approximately thirty minutes. This “conditioning period” is important to stimulate blood flow to the genital tissues. Once the “conditioning period” is complete, and additional blood flow has been stimulated, the user then applies the device only before vaginal sex. In the preferred method, the user applies the device approximately thirty minutes before engaging in vaginal sex to acutely increase blood flow and enhance sexual arousal. The user removes the device before vaginal sex.
Having thus described several aspects of at least one embodiment of this invention, it is to be appreciated various alterations, modifications, and improvements will readily occur to those skilled in the art. Such alterations, modifications, and improvements are intended to be part of this disclosure, and are intended to be within the spirit and scope of the invention. For example, the device may further include additional structures and elements to increase or enhance clitoral blood flow and stimulation. Such structures may include mechanical attachments secured to the device to contact the clitoral tissue without compressing, obstructing or pinching. Another embodiment may include vibratory devices secured to a portion of device body, and electronically or mechanically operated to enhance clitoral blood flow. Another embodiment may include the use of a heat-producing compound on a surface-contacting portion of the device to stimulate the user. All of these supplemental-structures may be used in combination with the vacuum producing device to increase the overall efficiency of the device and enhance stimulation of the user. Accordingly, the foregoing description and drawings are by way of example only.
| Number | Name | Date | Kind |
|---|---|---|---|
| 5813973 | Gloth | Sep 1998 | A |
| 6464653 | Hovland et al. | Oct 2002 | B1 |
| 6733438 | Dann et al. | May 2004 | B1 |
