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      Adherence to the International Committee of Medical Journal Editors’ (ICMJE) prospective registration policy and implications for outcome integrity: a cross-sectional analysis of trials published in high-impact specialty society journals

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          Abstract

          Background

          Registration of clinical trials is critical for promoting transparency and integrity in medical research; however, trials must be registered in a prospective fashion to deter unaccounted protocol modifications or selection of alternate outcomes that may enhance favorability of reported findings. We assessed adherence to the International Committee of Medical Journal Editors’ (ICMJE) prospective registration policy and identified the frequency of registrations occurring after potential observation of primary outcome data among trials published in the highest-impact journals associated with US professional medical societies. Additionally, we examined whether trials that are unregistered or registered after potential observation of primary outcome data were more likely to report favorable findings.

          Methods

          We conducted a retrospective, cross-sectional analysis of the 50 most recently published clinical trials that reported primary results in each of the ten highest-impact US medical specialty society journals between 1 January 2010 and 31 December 2015. We used descriptive statistics to characterize the proportions of trials that were: registered; registered retrospectively; registered retrospectively potentially after initial ascertainment of primary outcomes; and reporting favorable findings, overall and stratified by journal and trial characteristics. Chi-squared analyses were performed to assess differences in registration by journal and trial characteristics.

          Results

          We reviewed 6869 original research reports published between 1 January 2010 and 31 December 2015 to identify a total of 486 trials across 472 publications. Of these 486 trials, 47 (10%) were unregistered. Among 439 registered trials, 340 (77%) were registered prospectively and 99 (23%) retrospectively. Sixty-seven (68%) of these 99 retrospectively registered trials, or 15% of all 439 registered trials, were registered after potential observation of primary outcome data ascertained among participants enrolled at inception. Industry-funded trials, those with enrollment sites in the US, as well as those assessing FDA-regulated interventions each had lower rates of retrospective registration. Unregistered trials were more likely to report favorable findings than were registered trials (89% vs. 64%; relative risk (RR) = 1.38, 95% confidence interval (CI) = 1.20–1.58; p = 0.004), irrespective of registration timing.

          Conclusions

          Adherence to the ICMJE’s prospective registration policy remains sub-standard, even in the highest-impact journals associated with US professional medical societies. These journals frequently published unregistered trials and trials registered after potential observation of primary outcome data.

          Electronic supplementary material

          The online version of this article (10.1186/s13063-018-2825-y) contains supplementary material, which is available to authorized users.

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          Most cited references24

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          Clinical trial registration: a statement from the International Committee of Medical Journal Editors.

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            Comparison of registered and published primary outcomes in randomized controlled trials.

            As of 2005, the International Committee of Medical Journal Editors required investigators to register their trials prior to participant enrollment as a precondition for publishing the trial's findings in member journals. To assess the proportion of registered trials with results recently published in journals with high impact factors; to compare the primary outcomes specified in trial registries with those reported in the published articles; and to determine whether primary outcome reporting bias favored significant outcomes. MEDLINE via PubMed was searched for reports of randomized controlled trials (RCTs) in 3 medical areas (cardiology, rheumatology, and gastroenterology) indexed in 2008 in the 10 general medical journals and specialty journals with the highest impact factors. For each included article, we obtained the trial registration information using a standardized data extraction form. Of the 323 included trials, 147 (45.5%) were adequately registered (ie, registered before the end of the trial, with the primary outcome clearly specified). Trial registration was lacking for 89 published reports (27.6%), 45 trials (13.9%) were registered after the completion of the study, 39 (12%) were registered with no or an unclear description of the primary outcome, and 3 (0.9%) were registered after the completion of the study and had an unclear description of the primary outcome. Among articles with trials adequately registered, 31% (46 of 147) showed some evidence of discrepancies between the outcomes registered and the outcomes published. The influence of these discrepancies could be assessed in only half of them and in these statistically significant results were favored in 82.6% (19 of 23). Comparison of the primary outcomes of RCTs registered with their subsequent publication indicated that selective outcome reporting is prevalent.
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              Reproducible Research Practices and Transparency across the Biomedical Literature

              There is a growing movement to encourage reproducibility and transparency practices in the scientific community, including public access to raw data and protocols, the conduct of replication studies, systematic integration of evidence in systematic reviews, and the documentation of funding and potential conflicts of interest. In this survey, we assessed the current status of reproducibility and transparency addressing these indicators in a random sample of 441 biomedical journal articles published in 2000–2014. Only one study provided a full protocol and none made all raw data directly available. Replication studies were rare (n = 4), and only 16 studies had their data included in a subsequent systematic review or meta-analysis. The majority of studies did not mention anything about funding or conflicts of interest. The percentage of articles with no statement of conflict decreased substantially between 2000 and 2014 (94.4% in 2000 to 34.6% in 2014); the percentage of articles reporting statements of conflicts (0% in 2000, 15.4% in 2014) or no conflicts (5.6% in 2000, 50.0% in 2014) increased. Articles published in journals in the clinical medicine category versus other fields were almost twice as likely to not include any information on funding and to have private funding. This study provides baseline data to compare future progress in improving these indicators in the scientific literature.
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                Author and article information

                Contributors
                (484) 707-4114 , anand.gopal@yale.edu
                joshua.wallach@yale.edu
                jenerius.aminawung@yale.edu
                gregg.gonsalves@yale.edu
                rfdalre@gmail.com
                jennifer.miller@nyumc.org
                joseph.ross@yale.edu
                Journal
                Trials
                Trials
                Trials
                BioMed Central (London )
                1745-6215
                23 August 2018
                23 August 2018
                2018
                : 19
                : 448
                Affiliations
                [1 ]ISNI 0000000419368710, GRID grid.47100.32, Yale University School of Medicine, ; Harkness Hall, 367 Cedar Street, Box #415, New Haven, CT 06510 USA
                [2 ]ISNI 0000000419368710, GRID grid.47100.32, Center for Outcomes Research and Evaluation (CORE), Yale-New Haven Hospital and Collaboration for Research Integrity and Transparency, , Yale University, ; New Haven, CT USA
                [3 ]ISNI 0000000419368710, GRID grid.47100.32, Yale School of Public Health, ; New Haven, CT USA
                [4 ]ISNI 0000000119578126, GRID grid.5515.4, Epidemiology Unit, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid, ; Madrid, Spain
                [5 ]ISNI 0000 0004 1936 8753, GRID grid.137628.9, Division of Medical Ethics, Department of Population Health, , NYU School of Medicine, ; New York, NY USA
                [6 ]GRID grid.429057.d, Bioethics International, ; New York, NY USA
                [7 ]ISNI 0000000419368710, GRID grid.47100.32, Department of Internal Medicine, , Yale University School of Medicine, ; New Haven, CT USA
                Author information
                http://orcid.org/0000-0002-5386-5396
                Article
                2825
                10.1186/s13063-018-2825-y
                6106722
                30134950
                aa6a9256-e512-4819-a114-e74371c5d525
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 2 January 2018
                : 27 July 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100007184, Yale School of Medicine;
                Funded by: FundRef http://dx.doi.org/10.13039/100009827, Laura and John Arnold Foundation;
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Medicine
                trial registration,icmje,selective reporting
                Medicine
                trial registration, icmje, selective reporting

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