Quality and consistency of outcome reporting in clinical trials of immunosuppression in renal transplantation
Author:
Affiliation:
1. Nuffield Department of Surgical Sciences; University of Oxford; Oxford UK
2. Centre for Evidence in Transplantation; Clinical Effectiveness Unit; Royal College of Surgeons of England; London UK
Publisher
Wiley
Subject
Transplantation
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ctr.12837/fullpdf
Reference19 articles.
1. The quality of reporting of randomized controlled trials in solid organ transplantation;Pengel;Transpl Int,2009
2. Trial design and end points in clinical transplant research;Knight;Transpl Int,2016
3. Compliance to the CONSORT statement of randomized controlled trials in solid organ transplantation: a 3-year overview;Liu;Transpl Int,2013
4. CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials;Schulz;Int J Surg Lond Engl,2011
5. The impact of outcome reporting bias in randomised controlled trials on a cohort of systematic reviews;Kirkham;BMJ,2010
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1. Rabbit anti-thymocyte globulin (rATG) versus IL-2 receptor antagonist induction therapies in tacrolimus-based immunosuppression era: a meta-analysis;International Urology and Nephrology;2020-03-13
2. Evidence in Transplantation;Kidney Transplantation - Principles and Practice;2019
3. Range and Consistency of Outcomes Reported in Randomized Trials Conducted in Kidney Transplant Recipients: A Systematic Review;Transplantation;2018-12
4. Developing Consensus-Based Priority Outcome Domains for Trials in Kidney Transplantation;Transplantation;2017-08
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