Patient-important outcomes in registered diabetes trials

Gunjan Y. Gandhi, M. Hassan Murad, Akira Fujiyoshi, Rebecca J. Mullan, David N. Flynn, Mohamed B. Elamin, Brian A. Swiglo, William L. Isley, Gordon H. Guyatt, Victor M. Montori

Research output: Contribution to journalArticlepeer-review

170 Scopus citations


Context: Concerns about the safety and efficacy of diabetes interventions persist, in part because randomized clinical trials (RCTs) have not measured their effect on patient-important outcomes, ie, death and quality of life (morbidity, pain, function). Objective: To systematically determine the extent to which ongoing and future RCTs in diabetes will ascertain patient-important outcomes. Data Sources: On November 10, 2007, we searched primary RCT registries (, International Standard Randomized Controlled Trial Number Register (, and Australian New Zealand Clinical Trials Registry ( Study Selection: We identified phase 2 through 4 RCTs enrolling patients with diabetes. Of 2019 RCTs, 1054 proved eligible. We randomly sampled 50% of the eligible RCTs (527 of 1054) and selected 436 registered since registration became mandatory (2004). Data Extraction: Pairs of reviewers working independently collected study characteristics and determined the outcomes measured and their type (physiological outcomes, surrogate outcomes thought to reflect an increased risk for patient-important outcomes, and patient-important outcomes). Results: Of the 436 registered RCTs included in this analysis, 24 (6%) had not started enrollment, 109 (25%) were actively enrolling, and 303 (69%) had completed enrollment. Primary outcomes were patient-important outcomes in only 78 of 436 RCTs (18%; 95% confidence interval [CI], 14%-22%), physiological and laboratory outcomes in 69 of 436 (16%; 95% CI, 13%-20%), and surrogate outcomes in 268 of 436 (61%; 95% CI, 57%-66%). Patient-important outcomes were reported as primary or secondary outcomes in 201 of 436 (46%; 95% CI, 41%-51%). In multivariate analysis, large trials (odds ratio [OR], 1.10; 95% CI, 1.02-1.19 for every additional 100 patients) and trials of longer duration (OR, 1.03; 95% CI, 1.01-1.06 for every additional 30 days) were more likely while parallel design RCTs (OR, 0.15; 95% CI, 0.05-0.44) and type 2 diabetes trials (OR, 0.23; 95% CI, 0.09-0.61) were less likely to assess patient-important outcomes as a primary outcome. Conclusion: In this sample of registered ongoing RCTs in diabetes, only 18% included patient-important outcomes as primary outcomes.

Original languageEnglish (US)
Pages (from-to)2543-2549
Number of pages7
Issue number21
StatePublished - Jun 4 2008

ASJC Scopus subject areas

  • General Medicine


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