My expertise centers on adaptive and Bayesian clinical trials, which include platform trials; translational, clinical, health services, and outcomes research; interim data analysis; data monitoring committees; and informed consent in emergency research studies. These clinical trial designs use the incoming stream of information that exists during the conduct of a clinical trial to trigger changes in key clinical trial characteristics to improve the ethical balance, statistical efficiency, or scientific value of the trial relative to a fixed, non-adaptive trial design. Pubmed Bibliography.
18 December, 2024