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Improving the Reporting of Clinical Trials of Infertility Treatments (IMPRINT): modifying the CONSORT statement†‡
Author(s) -
Richard S. Legro,
Xiaoke Wu,
Kurt T. Barnhart,
Cindy Farquhar,
Bart C.J.M. Fauser,
Ben W. Mol,
Craig Niederberger,
Ernest Hung Yu Ng,
Stefano Palomba,
Afanador Rodríguez María,
Reggio Emilia,
Heping Zhang,
Robert W. Rebar,
Antonio Pellicer,
Richard H. Reindollar,
Juha S. Tapanainen,
J.L.H. Evers,
Seetha Shankaran,
Robert M. Silver,
Robert J. Norman,
Santanu Acharya,
Sheryl Vanderpoel,
Sheryl Vanderpool
Publication year - 2014
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/deu218
Subject(s) - medicine , infertility , live birth , clinical trial , consolidated standards of reporting trials , pregnancy , checklist , randomized controlled trial , reproductive medicine , obstetrics , psychology , surgery , genetics , cognitive psychology , biology
Clinical trials testing infertility treatments often do not report on the major outcomes of interest to patients and clinicians and the public (such as live birth) nor on the harms, including maternal risks during pregnancy and fetal anomalies. This is complicated by the multiple participants in infertility trials which may include a woman (mother), a man (father), and result in a third individual if successful, their offspring (child), who is also the desired outcome of treatment. The primary outcome of interest and many adverse events occur after cessation of infertility treatment and during pregnancy and the puerperium, which create a unique burden of follow-up for clinical trial investigators and participants. In 2013, because of the inconsistencies in trial reporting and the unique aspects of infertility trials not adequately addressed by existing Consolidated Standards of Reporting Trials (CONSORT) statements, we convened a consensus conference in Harbin, China, with the aim of planning modifications to the CONSORT checklist to improve the quality of reporting of clinical trials testing infertility treatment. The consensus group recommended that the preferred primary outcome of all infertility trials is live birth (defined as any delivery of a live infant ≥20 weeks gestations) or cumulative live birth, defined as the live birth per women over a defined time period (or number of treatment cycles). In addition, harms to all participants should be systematically collected and reported, including during the intervention, any resulting pregnancy, and during the neonatal period. Routine information should be collected and reported on both male and female participants in the trial. We propose to track the change in quality that these guidelines may produce in published trials testing infertility treatments. Our ultimate goal is to increase the transparency of benefits and risks of infertility treatments to provide better medical care to affected individuals and couples.

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