Guest guest Posted May 16, 2011 Report Share Posted May 16, 2011 Understanding Clinical Trial Design: A Tutorial for Research Advocates Authored by Jane Perlmutter, PhD for Research Advocacy Network's Advocate Institute Jane is also a participating patient advocate at CALGB http://fightcolorectalcancer.org/download/RAT2008/CTTutorial.pdf snip: Trade-offs in Designing Clinical Trials " Research advocates are increasingly playing an important role in designing clinical trials that are patient focused and likely to lead to important changes in clinical practice. We want to be sure that clinical trials are designed in a way that will lead to unequivocal results (i.e., are effective at answering research questions). However, we also want to be sure that trials can be completed as rapidly and inexpensively as possible (i.e., efficiently use resources), and that the patients who volunteer to be in trials get the best possible treatment (i.e., the trials achieve the highest ethical standards). These goals are often at cross purposes; thus, clinical trial designs generally represent a compromise. As shown in Figure 1 (page 2), in " Applies for any cancer type. Patients Against Lymphoma www.Lymphomation.org Evidence-based information on lymphoma, independent of health industry funding Quote Link to comment Share on other sites More sharing options...
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