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Registry-based randomised controlled trials – the future for clinical trials?
Session Moderator: Marion Campbell Professor of Health Services Research @MarionKCampbell
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Our challenge Cost of trials escalating
Trials seen to be burdensome to run; require stand alone infrastructure and lots of data collection The challenge… How can we evaluate rigorously BUT efficiently? Potential solution… Registry-based randomised controlled trials?
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What is a registry? “A patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves a predetermined scientific, clinical, or policy purpose(s)”…AHRQ
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What are Registry based trials?
Trials that are seamlessly nested onto the registry infrastructure Use the registry as a platform for data collection, follow up (and ideally) randomisation … the next “disruptive technology in clinical trials”?
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Content of session Overview of RRCTs?
Updates on international projects researching RRCTs Information on the practical liaison of trials with registries Using registries to track innovation for evaluation Discussion
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Speakers Prof Lehana Thabane, McMaster University, Canada
Dr Ted Lystig, Medtronic & CTTI initiative, US Prof David Beard, University of Oxford, UK Prof Jane Blazeby, University of Bristol, UK Open discussion
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