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Trial design and endpoints in clinical transplant research
Author(s) -
Knight Simon R.,
Morris Peter J.,
Schneeberger Stefan,
Pengel Liset H. M.
Publication year - 2016
Publication title -
transplant international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.998
H-Index - 82
eISSN - 1432-2277
pISSN - 0934-0874
DOI - 10.1111/tri.12743
Subject(s) - medicine , clinical trial , intensive care medicine , clinical study design , scope (computer science) , organ transplantation , transplantation , research design , clinical practice , quality (philosophy) , medical physics , pathology , surgery , family medicine , computer science , social science , philosophy , epistemology , sociology , programming language
Summary The number of clinical trials in solid organ transplantation is progressively increasing year on year, but the quality of design and reporting still varies considerably. The constraints on organ availability, improving short‐term outcomes, ethics and timescales involved in organ transplantation present unique challenges for trials in this field. An understanding of the methodology and potential pitfalls in clinical research is essential both to interpret trial results and to design robust studies. This review summarizes the scope and quality of reporting in existing transplant clinical trials and details aspects of clinical trial methodology with particular relevance to transplantation. We highlight initiatives designed to improve the quality of this process to ensure that the results of clinical trials are robust, well reported and of use in everyday clinical practice.

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