Participating in Multi-Center Clinical Trials

View webcast of Participating in Multi-Center Clinical Trials, originally produced in conjunction with the Society’s Women’s Leadership Initiative.

This webcast of a Heart Rhythm 2008 session includes details for identifying and becoming involved in multi-institution clinical trials, the process of using clinical trial data for sub-study analysis and hypothesis-generating for future prospective trials and more.

Chair
Jeanne E. Poole, MD

Faculty

• The Language of the NIH: Types of Studies, NIH Funding and the NIH Process (presentation length, 20:28)
  Alice M. Mascette, MD
  Chief, Heart Failure & Arrhythmias Branch
  Bethesda, MD
  
• The Devil is in the Details: The IRB and Other Site Study Issues (presentation length, 14:59)
  Karen J. Friday, MD
  Stanford University School of Medicine
  Palo Alto, CA
  
• Breaking into Clinical Trial Participation: Substudies, Committees and Becoming a Site Investigator (presentation length, 16:55)
  Marye J. Gleva MD
  Clinical Electrophysiology Laboratory
  Washington University in St. Louis School of Medicine
  St. Louis, MO
  
• Tools of the Trade: Statistical Realities (presentation length, 17:13)
  Christine M. Albert, MD, MPH
  Director, Center for Arrhythmia Prevention
  Cardiac Arrhythmia Service
  Brigham and Women’s Hospital
  Boston, MA
• Clinical Trials Wrap-Up (presentation length, 22:25)
  Jeanne E. Poole, MD
  Professor of Medicine and Director, Arrhythmia Service and Electrophysiology Laboratory
  University of Washington Medical Center
  Seattle, WA

View Webcast
Participating in Multi-Center Clinical Trials