Clinical trial design/analysis in traumatic brain injury

Information

  • Research Project
  • 6881189
  • ApplicationId
    6881189
  • Core Project Number
    R01NS042691
  • Full Project Number
    5R01NS042691-03
  • Serial Number
    42691
  • FOA Number
  • Sub Project Id
  • Project Start Date
    2/15/2003 - 22 years ago
  • Project End Date
    1/31/2007 - 18 years ago
  • Program Officer Name
    GILBERT, PETER R
  • Budget Start Date
    2/1/2005 - 20 years ago
  • Budget End Date
    1/31/2007 - 18 years ago
  • Fiscal Year
    2005
  • Support Year
    3
  • Suffix
  • Award Notice Date
    2/10/2005 - 20 years ago

Clinical trial design/analysis in traumatic brain injury

DESCRIPTION (provided by the applicant): Traumatic brain injury (TBI) constitutes a major health and socio-economic problem throughout the world, accounting for a third of trauma deaths and for a much larger proportion of life-long disability after trauma. Despite enthusiasm generated from positive pre-clinical investigations, and of phase II trials on new therapies for reducing secondary brain damage and improving outcome, the results of phase III trials have been extremely disappointing, none of them showing convincing evidence of efficacy in the overall population of TBI. Problems in clinical trial design and analysis, specific to the field of TBI, have contributed to this failure. Methodologic challenges are related to the heterogeneity of the population, outcome assessment, detection of treatment effects, the use of surrogate markers and interim analysis. Addressing these problems requires a multidisciplinary effort involving expertise from the fields of clinical research, biostatistics and epidemiology. This effort is realized in the proposed study, organized as an international collaboration, based on extensive analysis of data available from studies (n=3) and trials (n=8) in TBI, encompassing approximately 10,000 patients. The efficiency of mechanistic and/or prognostic targeting, as well as covariate adjustment for dealing with heterogeneity, will be investigated (spec. aim 1), influence of outcome distribution and observer variation on statistical power, differentiated analysis of outcome according to prognostic risk (spec. aim 2), and development/validation of prognostic models with conventional statistical approaches, as well as with approaches new to the field of TBI (spec. aim 3). Additional design issues, considered relevant to TBI trials, focusing on recruitment, time-windows, and sequential design are addressed (spec. aim 4). The insight obtained from these investigations will lead to informed recommendations for the design and analysis of future clinical trials. Results may also be relevant to trials in other fields of medicine, in which similar problems have been recognized, such as stroke, sepsis and ARDS. The global aim is to optimize chances for demonstrating benefit of an effective new therapy or therapeutic agent in the field of TBI.

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    R01
  • Administering IC
    NS
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    472354
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    853
  • Ed Inst. Type
  • Funding ICs
    NINDS:472354\
  • Funding Mechanism
  • Study Section
    NSD
  • Study Section Name
    National Institute of Neurological Disorders and Stroke Initial Review Group
  • Organization Name
    ERASMUS UNIVERSITY OF ROTTERDAM
  • Organization Department
  • Organization DUNS
  • Organization City
    ROTTERDAM
  • Organization State
  • Organization Country
    NETHERLANDS
  • Organization Zip Code
  • Organization District
    NETHERLANDS