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European Journal of Clinical Pharmacology|August 4, 2016
Prevention of selective outcome reporting: let us start from the beginningRafael Dal-Ré, Ana MarušićEuropean Journal of Clinical Investigation|June 26, 2015
Journal editors impasse with outcome reporting biasRafael Dal-Ré, Arthur L CaplanEuropean Journal of Clinical Pharmacology|August 15, 2023
Posting of clinical trial results and other critical information from completed medicines trials on ClinicalTrials.govRafael Dal-Ré, Ignacio Mahillo-FernándezThe AAPS Journal|June 18, 2024
Principal Features of Industry-Funded Trials that Posted Informed Consent Forms on ClinicalTrials.gov: a Cross-Sectional AnalysisRafael Dal-Ré, Ignacio Mahillo-FernándezEuropean Journal of Clinical Pharmacology|January 14, 2014
Time to ensure that clinical trial appropriate results are actually publishedRafael Dal-Ré, Arthur L CaplanTrials|March 30, 2017
Why prudence is needed when interpreting articles reporting clinical trial results in mental healthRafael Dal-Ré, Julio Bobes, Pim CuijpersGaceta Sanitaria|December 1, 2014
[Registration of observational studies: it is time to comply with the Declaration of Helsinki requirement]Rafael Dal-Ré, Miguel Delgado, Francisco BolumarMedicina Clinica|December 21, 2004
Nature and extent of changes in the patient's information sheets of international multicentre clinical trials as requested by Spanish Research Ethics CommitteesRafael Dal-Ré, Elena Morejón, Rafael OrtegaJournal of Medical Ethics|May 23, 2022
Equipoise, standard of care and consent: responding to the authorisation of new COVID-19 treatments in randomised controlled trialsSoren Holm, Jonathan Lewis, Rafael Dal-RéJournal of Clinical Epidemiology|January 29, 2016
Compliance with prospective trial registration guidance remained low in high-impact journals and has implications for primary end point reportingRafael Dal-Ré, Joseph S Ross, Ana MarušićPageof 9