dc.contributor.author | Murad, M. H. | |
dc.contributor.author | Guyatt, G. H. | |
dc.contributor.author | Domecq, J. P. | |
dc.contributor.author | Vemooij, R. W. M. | |
dc.contributor.author | Erwin, P. J. | |
dc.contributor.author | Meerpohl, J. J. | |
dc.contributor.author | Prutsky, G. J. | |
dc.contributor.author | Akl, E. A. | |
dc.contributor.author | Mueller, K. | |
dc.contributor.author | Bassler, D. | |
dc.contributor.author | Schandelmaier, S. | |
dc.contributor.author | Walter, S. D. | |
dc.contributor.author | Busse, J. W. | |
dc.contributor.author | Kasenda, B. | |
dc.contributor.author | Pagano, G. | |
dc.contributor.author | Pardo-Hernandez, H. | |
dc.contributor.author | Montori, V. M. | |
dc.contributor.author | Wang, Z. | |
dc.contributor.author | Briel, M. | |
dc.date.accessioned | 2019-01-25T16:36:28Z | |
dc.date.available | 2019-01-25T16:36:28Z | |
dc.date.issued | 2017 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/4839 | |
dc.description.abstract | Objective: We explored how investigators of ongoing or planned trials respond to the publication of a trial stopped early for benefit addressing a similar question. Study Design and Setting: We searched multiple databases from the date of publication of the truncated trial through August, 2015. Independent reviewers selected trials and extracted data. Results: We identified 207 trials truncated for early benefit; of which 102 (49%) were followed by subsequent trials (262 subsequent trials, median 2 per truncated trial, range 1-13). Only 99 (38%) provided a rationale justifying conducting a trial despite prior stopping. The top reasons were to address different population or setting (33%), skepticism of truncated trials findings because of small sample size (12%), inconsistency with other evidence (11%), or increased risk of bias (7%). We did not identify significant associations between subsequent trials and characteristics of truncated ones (risk of bias, precision, funding, or rigor of stopping decision). Conclusion: About half of the trials stopped early for benefit were followed by subsequent trials addressing a similar question. This suggests that future trialists may have been skeptic about the decision to stop prior trials. A more rigorous threshold for stopping early for benefit is needed. | en_US |
dc.language.iso | eng | |
dc.publisher | Elsevier | |
dc.relation.ispartofseries | Journal of Clinical Epidemiology | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | Health | en_US |
dc.subject | Public, Environmental & Occupational | en_US |
dc.subject | Health Care Sciences & Services | en_US |
dc.subject | Systematic review | en_US |
dc.subject | clinical-trial | en_US |
dc.subject | critically-ill patients | en_US |
dc.subject | Early | en_US |
dc.subject | intensive insulin therapy | en_US |
dc.subject | Methodology | en_US |
dc.subject | Randomized controlled trials | en_US |
dc.subject | termination of trials | en_US |
dc.subject | Trial design | en_US |
dc.subject | Trials stopped early for benefit | en_US |
dc.title | Randomized trials addressing a similar question are commonly published after a trial stopped early for benefit | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1016/j.jclinepi.2016.10.006 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.03.09 | |
dc.relation.issn | 1878-5921 |
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