Showing items related by title, author, creator and subject.

• Challenges to Effective Research in Acute Trauma Resuscitation: Consent and Endpoints 

  Holcomb, John B; Weiskopf, Richard; Champion, Howard; Gould, Steven A; Sauer, R Michelle; Brasel, Karen; Bochicchio, Grant; Bulger, Eileen; Cotton, Bryan A; Davis, Daniel; Dutton, Richard; Hauser, Carl J; Hess, John R; Hides, George A; Knudson, Paula; MacKenzie, Ellen; McGinnis, Robert L; Michalek, Joel; Moore, Frederick A; Omert, Laurel; Pollock, Brad H; Tortella, Bartholomew; Sugarman, Jeremy; Schreiber, Martin A; Wade, Charles E (2011-02)

  Selection of study endpoints is one of the most important decisions in the design of effective clinical trials. Late mortality (e.g., 28 days) is an unambiguous endpoint, accepted by regulatory agencies, but it is viewed ...
• A Geospatial Analysis of Persons Opting Out of an Exception From Informed Consent Out-of-Hospital Clinical Trial 

  Nelson, Maria J.; Warden, Craig; Griffiths, Denise; Zive, Dana; Schmidt, Terri; Hedges, Jerris R.; Daya, Mohamud; Newgard, Craig D. (2009-01)
• Conducting Research Using the Emergency Exception From Informed Consent: The Public Access Defibrillation (PAD) Trial Experience 

  Mosesso, Vincent N., Jr.; Brown, Lawrence H.; Greene, H. Leon; Schmidt, Terri A.; Aufderheide, Tom P.; Sayre, Michael R.; Stephens, Shannon W.; Travers, Andrew; Craven, Richard A.; Weisfeldt, Myron L. (Public Access Defibrillation [PAD] Trial Investigators, 2004-04)