A systematic approach to all aspects of designing andconducting clinical trialsThe success or failure of clinical trials hinges on hundreds ofdetails that need to be developed, often under less than idealconditions. Written by one of the world's leading trialists,Clinical Trials Handbook: Design and Conduct providesclinicians with a complete guide to designing, conducting, andevaluating clinical trials--teaching them how to simplify theprocess and avoid costly mistakes.The author draws on his extensive clinical trials experience tooutline all steps employed in setting up and running clinicaltrials, from budgeting and fundraising to publishing the results.Along the way, practical advice is offered while also addressing amix of logistical, ethical, psychological, behavioral, andadministrative issues inherent to clinical trials. Topics ofcoverage include:* Protocols for drug masking, controls, and treatmentrandomization* Consent, enrollment, eligibility, and follow-up procedures* Different types of sample size design and data collection andprocessing* Working with study centers, research staff, and variouscommittees* Monitoring treatment effects and performance, and ensuringquality control* Data analysis and access policies for study data anddocumentsClinical Trials Handbook is invaluable for practicingclinicians and trialists who would like to learn more about orimprove their understanding of the design and execution of clinicaltrials. The book is also an excellent supplement for courses onclinical trials at the graduate level.