Association between trial registration and treatment effect estimates: a meta-epidemiological study
© The Author(s). 2016
Received: 29 March 2016
Accepted: 8 June 2016
Published: 4 July 2016
To increase transparency in research, the International Committee of Medical Journal Editors required, in 2005, prospective registration of clinical trials as a condition to publication. However, many trials remain unregistered or retrospectively registered. We aimed to assess the association between trial prospective registration and treatment effect estimates.
This is a meta-epidemiological study based on all Cochrane reviews published between March 2011 and September 2014 with meta-analyses of a binary outcome including three or more randomised controlled trials published after 2006. We extracted trial general characteristics and results from the Cochrane reviews. For each trial, we searched for registration in the report’s full text, contacted the corresponding author if not reported and searched ClinicalTrials.gov and the International Clinical Trials Registry Platform in case of no response. We classified each trial as prospectively registered (i.e. registered before the start date); retrospectively registered, distinguishing trials registered before and after the primary completion date; and not registered. Treatment effect estimates of prospectively registered and other trials were compared by the ratio of odds ratio (ROR) (ROR <1 indicates larger effects in trials not prospectively registered).
We identified 67 meta-analyses (322 trials). Overall, 225/322 trials (70 %) were registered, 74 (33 %) prospectively and 142 (63 %) retrospectively; 88 were registered before the primary completion date and 54 after. Unregistered or retrospectively registered trials tended to show larger treatment effect estimates than prospectively registered trials (combined ROR = 0.81, 95 % CI 0.65–1.02, based on 32 contributing meta-analyses). Trials unregistered or registered after the primary completion date tended to show larger treatment effect estimates than those registered before this date (combined ROR = 0.84, 95 % CI 0.71–1.01, based on 43 contributing meta-analyses).
Lack of trial prospective registration may be associated with larger treatment effect estimates.
KeywordsBias Registration ClinicalTrials.gov Meta-epidemiology Randomised controlled trial Meta-analysis
In 2005, the International Committee of Medical Journal Editors (ICMJE) initiated a policy for trial registration to increase transparency in research. All trials that started recruiting on or after 1 July 2005 should be registered prospectively (i.e. before participant enrolment) as a precondition for publication in member journals . Trials that started recruitment before this date should be registered retrospectively but before 13 September 2005. The World Health Organisation announced its support for trial registration and launched the International Clinical Trials Registry Platform (ICTRP) to facilitate access to existing registries worldwide [2, 3]. These announcements were followed by a massive increase in trial registration that became the norm rather than the exception [3, 4]. However, a substantial proportion of trials remain unregistered. A study published in 2009 found that 28 % of trials published in the 10 general medical and specialty journals with the highest impact factor were not registered . Another found that 39 % of published trials retrieved from MEDLINE appeared not to have been registered .
Recently, some researchers generated an important debate among the medical community, arguing that trials published after 2010 that are not prospectively registered should be excluded from Cochrane reviews . Registration aims to make information about the existence and methods of clinical trials publicly available to limit the effect of selective publication of trials and outcomes with positive results resulting in exaggerated treatment effect estimates [8–13]. However, the evidence is as yet unclear concerning a possible association between trial registration and treatment effect estimates .
In this study, we aimed to investigate whether there is a difference in treatment effect estimates according to trial prospective registration.
We performed a meta-epidemiological study. By using large collections of meta-analyses, these studies are used to assess the association between a trial characteristic and treatment effect estimates [15–18]. For this study, we focussed on Cochrane systematic reviews including randomised controlled trials (RCTs) with results published in 2006 or after. We chose 2006 because registration was required by the ICMJE from September 2005.
We obtained data from all intervention systematic reviews published between March 2011 and September 2014 from the Cochrane Collaboration. Data were provided as XML files and consisted of all elements entered by the review authors in RevMan, the software developed by the Cochrane Collaboration for preparing and maintaining Cochrane reviews. Then, we applied the following selection criteria to perform the meta-epidemiological analyses.
Identification of relevant systematic reviews
Using R 3.1.1 with the XML package, we automatically identified all reviews of RCTs with meta-analyses of a binary outcome including three or more RCTs published after 2006. Reviews including observational studies were not considered.
Selection of relevant meta-analyses
From the reviews identified, we manually screened all eligible meta-analyses and selected those comparing an active treatment to a placebo or no treatment. Comparisons of two active interventions and meta-analyses of side effects were excluded because of the uncertainty regarding the direction of the bias. If several meta-analyses were eligible per review, we selected, whenever possible, the first meta-analysis including at least four trials (three trials is the minimum to perform meta-epidemiological analyses, four trials allows more power). In case of overlapping meta-analyses across reviews, defined as meta-analyses sharing three or more trials, we selected the one with the largest number of trials, and if they included the same number of trials, we selected the most recent one.
Selection of trials
All trials included in the selected meta-analyses were included in the study. RCTs without any events in both arms did not contribute to the analysis.
Data available from Cochrane reviews
The following data were automatically extracted by using R 3.1.1 with the XML package.
Review and meta-analysis characteristics
These characteristics included date of publication, medical condition and, for the selected meta-analysis, interventions being compared and outcome assessed.
Trial general characteristics and results
Reference of the publication identified from the ʻreferences to studies included in the review’.
Risk of bias assessment: judgment of bias (i.e. high, low or unclear risk of bias) for each domain of the Cochrane Collaboration Risk of Bias tool and the support for judgment. Because the wording of domains may vary across reviews (e.g. allocation concealment, allocation concealment [selection bias], sequence concealment), we pre-sorted all wording reported in the reviews and manually classified them. According to the Cochrane handbook, the blinding and incomplete outcome data domains should be assessed at the outcome level; therefore, for reviews reporting an evaluation of these domains by outcome or type of outcome, we manually identified the outcome corresponding to the selected meta-analysis.
Results: for each arm, the number of events as well as the number of patients analysed.
We manually searched the full text of each included review for any information regarding registration from the characteristics of included studies and the domains of the Risk of Bias tool: ʻselective outcome reporting’ and ʻother bias’.
If no information was reported in the review, we searched for the trial publication abstract and screened whether a registration number was reported.
If no information was reported, we searched Google for the publication title with key-words related to registration (i.e. registration, ClinicalTrials.gov, registered, NCT). If there was no result, we retrieved and screened the full text of the publication.
For trials for which we were unable to find any information regarding registration, we contacted the corresponding author to ask whether the trial was registered and, if so, in which registry and under which number.
In case of no response from the author, two reviewers independently searched ClinicalTrials.gov and the ICTRP using the trial acronym, if any, and keywords concerning population and experimental intervention. All disagreements on trial matching were resolved by consensus. A senior researcher (AD) checked the matching between each trial and registration information.
We classified each trial as (1) prospectively registered, defined as registered before or within a month of the start date (i.e. the date that enrolment to the protocol begins). The ICMJE considers that registration should occur before the start date, whereas the FDA considers that registration should occur within 21 days after the start date. Our definition is in accordance with these statements and takes into account the uncertainty regarding the exact start date, because for most trials, only month and year are reported; (2) retrospectively registered, defined as registered more than 1 month after the start date. We distinguished trials registered before and after the primary completion date (defined as the date of final collection of data for the primary outcome) because we made the assumption that registration after primary completion date could be influenced by the potential knowledge of the results and that it could result in more bias; or (3) not registered.
We also classified trials by compliance with the ICMJE requirements . Trials starting before July 2005 were considered compliant if they were registered before 13 September 2005 and trials starting in July 2005 or later were considered compliant if they were prospectively registered .
We estimated treatment outcomes as odds ratios (ORs). Outcome events were re-coded so that an OR <1 indicated a beneficial association with the experimental intervention.
Prospectively registered and other trials (i.e. unregistered, retrospectively registered and those for which this information was not reported) which is defined as the primary analysis.
Trials registered before the primary completion date and registered after or unregistered. Because we had missing data on primary completion date or completion date, we performed two different analyses. In the first analysis, we considered trials for which the primary completion date or completion date was not reported as missing data and did not take them into account in the analysis. In the second analysis, we assumed that trials not reporting the primary completion date were registered after the primary completion date (worst-case scenario).
Trials compliant and not compliant with the ICMJE requirement as defined above.
Registered and unregistered trials.
For each comparison, we used the following two-step approach described by Sterne et al. . First, for each meta-analysis, we estimated a ratio of odds ratio (ROR) by using a random-effects meta-regression. For the first comparison, for example, this is the ratio of the OR in unregistered or retrospectively registered RCTs to that in prospectively registered RCTs. An ROR <1 indicates larger treatment effect estimates for unregistered or retrospectively registered than prospectively registered trials. Second, we estimated a combined ROR across meta-analyses and the 95 % CI by using a random-effects meta-analysis model. The heterogeneity across meta-analyses was quantified with the I2 statistic and the between–meta-analysis variance τ2.
All analyses involved the use of Stata SE 11.0 (StataCorp, College Station, TX).
Selection and characteristics of systematic reviews
Overall, 53 meta-analyses assessed a pharmacological intervention for a total of 265 trials and 14 assessed a non-pharmacological intervention for a total of 57 trials.
Registration of included trials
Characteristics of included trials by registration status
N = 225
N = 97
N = 74
Retrospectively before PCDb
N = 88
Retrospectively after PCDb
N = 54
N = 9
Type of interventiona
Pharmacological (N = 265)
Non-pharmacological (N = 57)
2006–2009 (N = 169)
2010–2014 (N = 153)
Before July 2005 (N = 162)
In July 2005 or after (N = 133)
Not reported (N = 27)
Non-profit (N = 154)
Industry (N = 104)
Both (N = 22)
Not reported (N = 42)
Risk of bias
Sequence generation (high/unclear)
Allocation concealment (high/unclear)
Incomplete outcome data (high/unclear)
Comparison of treatment effect estimates between prospectively registered and unregistered or retrospectively registered trials
Comparison of treatment effect estimates between trials registered before primary completion date and those registered after or not registered
Comparison of treatment effect estimates between trials compliant and not compliant with the ICMJE requirement
From 42 meta-analyses (207 RCTs), we found a combined ROR = 0.86 (95 % CI 0.71–1.05) with larger estimates in trials not compliant to the ICMJE requirement; heterogeneity across meta-analyses was I2 = 36.6 %, τ2 = 0.1286 (Fig. 3).
Comparison of treatment effect estimates between unregistered and registered trials
From 37 meta-analyses (177 trials), the combined ROR between unregistered and registered trials was 0.85 (95 % CI: 0.67–1.08) with I2 = 37.2 % and τ2 = 0.1591 (Fig. 3).
With this study, we aimed to provide some evidence concerning the association between trial registration and treatment effect estimates. From a sample including all Cochrane reviews with trials published in 2006 or after, our results suggest that trials retrospectively registered or not registered may show larger treatment effect estimates than other trials. All analyses gave consistent results.
This is the first meta-epidemiological study assessing the association between trial registration and treatment effects. Meta-epidemiological studies are considered the gold standard for assessing bias . To determine whether a trial was registered, we used a sequential approach involving contacting corresponding authors and a duplicate search of registries in case of lack of information in trial reports. Because assessing the impact of prospective registration is complex in that it became a requirement for trials starting after July 2005, we conducted several complementary analyses (e.g. registration after the primary completion date, compliance with the ICMJE requirement), all of which gave consistent results with a trend to larger treatment effect estimates for unregistered trials and those retrospectively registered or registered after the primary completion date.
Two previous studies compared the conclusions of trials by registration status in specific medical areas [19, 20]. One found that trials registered before publication and those unregistered were equally likely to reach conclusions favouring new oncology drugs . A more recent study found that trials in cardiology reported as registered were less likely to report positive findings than those not reported as registered . Our results suggest that trial registration is an important element to consider because it may be associated with treatment effect estimates using a meta-epidemiological approach. Results from meta-epidemiological studies were used to determine the items associated with treatment effect estimates that could be related to bias and served as a basis to develop the Cochrane Risk of Bias tool [15, 16]. Meta-epidemiological studies have identified other characteristics not directly associated with a bias-producing process in an individual trial but manifesting when looking at collections of trials. Such characteristics including funding sources, single-centre status or sample size have been considered meta-bias . Trial registration may be another type of meta-bias.
Our study has some limitations. To perform the meta-epidemiological analysis, we had to predefine relatively restrictive selection criteria (i.e. selection of meta-analyses involving three RCTs or more), which resulted in a limited number of meta-analyses that may not be representative of all Cochrane reviews. Our analyses may lack power and we could only observe a trend but no statistically significant results, so our results should be interpreted carefully. We did not perform a formal sample size calculation because this is complex for meta-epidemiological studies and because of the uncertainty regarding the amount of difference in treatment effect estimates by registration status . We used all meta-analyses corresponding to our eligibility criteria from our sample of Cochrane reviews and reported the results transparently. We did not attempt to increase our sample size a posteriori because this would have been driven by our results. Such post hoc decisions are criticised and may result in overestimated associations. Even if we had found a statistical difference, we think that this would not be sufficient to justify decisions regarding the exclusion of trials from Cochrane reviews based on their registration status. This rather highlights the importance of systematically collecting this item and performing sensitivity analyses when conducting meta-analyses to assess whether it could affect the results. The number of meta-analyses and the number of trials per meta-analysis also limit the ability to explore whether meta-confounding by trial funding sources, sample size and risk of bias could explain our results because these characteristics are frequently associated with treatment effect estimates. Industry-sponsored trials are more likely to comply with registration policies than non-profit-funded trials [23–25] and also more likely to show more favourable results . Smaller trials or trials at high risk of bias might be more likely to be retrospectively registered or unregistered. Nevertheless, it has to be noted that most meta-epidemiological studies do not adjust on possible confounding factors .
A first implication for future research is to confirm our results in larger meta-epidemiological studies that could also allow adjustment for important confounding factors like funding source or sample size.
Other important implications can be discussed. Our results remind us of the importance of prospective registration for all trials which should be systematically verified by peer reviewers and editors during the peer review process. We suggest a careful interpretation of trials not registered or retrospectively registered, particularly those registered after the primary completion date. At the systematic review level, there is a need for systematically collecting and reporting information on trial registration for each included trial, which is currently not frequently done in systematic reviews. Although it is recommended to systematically report this information in reports of RCTs [28, 29], the PRISMA Statement [30, 31] and the Cochrane Handbook  do not contain recommendations for collecting and reporting this information when conducting a systematic review. Accounting for trial registration during the meta-analysis process is challenging. Our results cannot allow for recommending the exclusion of trials not registered or retrospectively registered from meta-analyses. Nevertheless, some arguments suggest that this approach is not appropriate, as it may lead to the exclusion of more recent trials and of trials funded by academic sources as they are less likely than industry-funded trials to comply with registration policy [23–25]. We rather recommend that review authors conduct sensitivity analyses based on registration status to check whether it has an influence on the results.
Our results suggest that trial registration may be associated with treatment effect estimates, with a tendency for larger effects in unregistered or retrospectively registered trials. Our results should be confirmed in other meta-epidemiological studies but highlight the importance of prospective registration for all trials.
CI, confidence interval; ICMJE, International Committee of Medical Journal Editors; ICTRP, International Clinical Trials Registry Platform; OR, odds ratio; RCT, randomised controlled trial; ROR, ratio of odds ratio
- Elise Diard for help with figures;.
- Valentin Faugeroux, Marina Dockes and Louis-Marie Lamar for help with data extraction;
- Mickael Randrianandrasana for help with data management;
- Raphael Porcher for helpful comments;
- David Tovey, editor in chief of the Cochrane Library, for having accepted to share data from Cochrane reviews, Javier Mayoral Campos, system administrator, Cochrane Central Executive for preparing files and all Cochrane reviewers who collected data.
The researchers did not receive external sources of funding. This work was internally funded by Cochrane France.
Availability of data and materials
The data are available to academic researchers upon request.
IB, AD and PR designed the study. AD and IA screened relevant studies. AD and CR extracted data. AD performed the statistical analysis. AD, IB and PR interpreted the results. AD and IB wrote the article. All authors critically reviewed the manuscript. AD is the guarantor. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
Ethics approval is not applicable. This study is a research on research study.
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.
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