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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.

Original publication




Journal article


Transpl Int

Publication Date





870 - 879


PICO, clinical trials, evidence, outcomes, randomized controlled trial, Clinical Trials as Topic, Endpoint Determination, Evidence-Based Medicine, Graft Survival, Humans, Organ Transplantation, Random Allocation, Research Design, Time Factors