Improving outcome reporting in clinical trial reports and protocols: study protocol for the Instrument for reporting Planned Endpoints in Clinical Trials (InsPECT) — Nancy J. Butcher (2019) | RDL Network
Improving outcome reporting in clinical trial reports and protocols: study protocol for the Instrument for reporting Planned Endpoints in Clinical Trials (InsPECT)
Article 2019 en
Authors
NB
Nancy J. Butcher
AM
Andrea Monsour
EM
Emma J. Mew
Abstract
1 min read
InsPECT will provide evidence-informed and consensus-based standards focused on outcome reporting in clinical trials that can be applied across diverse disease areas, study populations, and outcomes. InsPECT will support the standardization of trial outcome reporting, which will maximize trial usability, reduce bias, foster trial replication, improve trial design and execution, and ultimately reduce research waste and help improve patient outcomes.
Michael B. Smith, David Moher, Andrea Monsour, Leena Saeed, A.-W. Chan, Sunita Vohra, Martin Offringa, Suneeta Monga, Nancy J. Butcher, Wendy J. Ungar, Paula Williamson, Akira Baba, Evan Mayo‐Wilson, Robert Golub, L. Thabane, Péter Szatmári, Lisa Askie, Peter Tugwell, Emma J. Mew, Jeremy Grimshaw, F. Gavin, Lauren E. Kelly, Alyssandra Chee-A-Tow, Caroline B. Terwee,
Peter Tugwell, Andrea Monsour, Susan Marlin, Evan Mayo‐Wilson, Suneeta Monga, Alyssandra Chee-A-Tow, Paula Williamson, Robert Golub, Lehana Thabane, Nancy J. Butcher, Martin Offringa, Caroline B. Terwee, Jeremy Grimshaw, Akira Baba, Mufiza Farid‐Kapadia, Péter Szatmári, A.-W. Chan, Wendy J. Ungar, Leena Saeed, David Moher, Emma J. Mew, Lisa Askie, Lauren E. Kelly, Maureen A. Smith,
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