ReviewSystematic reviews2018
The use of clinical study reports to enhance the quality of systematic reviews: a survey of systematic review authors.
Review in Systematic reviews, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
21 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Pooled it
- Article
- Antipsychotics for Parkinson's disease: a protocol for a systematic review with network meta-analysis and trial sequential analysis.BMJ open · 2025Article
- Liberal Versus Restrictive Oxygenation Targets in Acute Heart Failure-A Protocol for a Systematic Review With Meta-Analysis.Acta anaesthesiologica Scandinavica · 2025Article
- A New Process Model of Study Identification Specific to the Identification of Randomised Studies for Systematic Reviews of Medical Interventions.Cochrane evidence synthesis and methods · 2025Article
- Adverse effects with tirzepatide: a protocol for a systematic review with meta-analysis and Trial Sequential Analysis.BMJ open · 2025Article
- Adverse effects with semaglutide: a protocol for a systematic review with meta-analysis and trial sequential analysis.BMJ open · 2024Article
- How to use the regulatory data from Health Canada for secondary analyses on new drugs, biologics and vaccines.BMJ evidence-based medicine · 2024Article
- A 10-year update to the principles for clinical trial data sharing by pharmaceutical companies: perspectives based on a decade of literature and policies.BMC medicine · 2023Article
- Conducting separate reviews of benefits and harms could improve systematic reviews and meta-analyses.Systematic reviews · 2023Article
- Bleeding Patterns of Oral Contraceptives with a Cyclic Dosing Regimen: An Overview.Journal of clinical medicine · 2022Review
- Article
- Optimizing the data available via Health Canada's clinical information portal.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2021Article
- Exploring the Food and Drug Administration's review and approval of Entresto (sacubitril/valsartan).Pharmacology research & perspectives · 2021Review
- Reporting of harms in oncological clinical study reports submitted to the European Medicines Agency compared to trial registries and publications-a methodological review.BMC medicine · 2021Article
- PRISMA-S: an extension to the PRISMA statement for reporting literature searches in systematic reviewsJournal of the Medical Library Association : JMLA · 2021Article
- PRISMA-S: an extension to the PRISMA Statement for Reporting Literature Searches in Systematic Reviews.Systematic reviews · 2021Article
- Efficacy and safety of sacubitril/valsartan in the treatment of heart failure: protocol for a systematic review incorporating unpublished clinical study reports.HRB open research · 2020Article
- European Medicines Agency Policy 0070: an exploratory review of data utility in clinical study reports for academic research.BMC medical research methodology · 2019Review
- Design characteristics, risk of bias, and reporting of randomised controlled trials supporting approvals of cancer drugs by European Medicines Agency, 2014-16: cross sectional analysis.BMJ (Clinical research ed.) · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
backgroundClinical study reports (CSRs) are produced for marketing authorisation applications. They often contain considerably more information about, and data from, clinical trials than corresponding journal publications. Use of data from CSRs might help circumvent reporting bias, but many researchers appear to be unaware of their existence or potential value. Our survey aimed to gain insight into the level of familiarity, understanding and use of CSRs, and to raise awareness of their potential within the systematic review community. We also aimed to explore the potential barriers faced when obtaining and using CSRs in systematic reviews.
methodsOnline survey of systematic reviewers who (i) had requested or used CSRs, (ii) had considered but not used CSRs and (iii) had not considered using CSRs was conducted. Cochrane reviewers were contacted twice via the Cochrane monthly digest. Non-Cochrane reviewers were reached via journal and other website postings.
resultsOne hundred sixty respondents answered an open invitation and completed the questionnaire; 20/160 (13%) had previously requested or used CSRs and other regulatory documents, 7/160 (4%) had considered but not used CSRs and 133/160 (83%) had never considered this data source. Survey respondents mainly sought data from the European Medicines Agency (EMA) and/or the Food and Drug Administration (FDA). Motivation for using CSRs stemmed mainly from concerns about reporting bias 11/20 (55%), specifically outcome reporting bias 11/20 (55%) and publication bias 5/20 (25%). The barriers to using CSRs noted by all types of respondents included current limited access to these documents (43 respondents), the time and resources needed to obtain and include these data in evidence syntheses (n = 25) and lack of guidance about how to use these sources in systematic reviews (n = 26).
conclusionsMost respondents (irrespective of whether they had previously used them) agreed that access to CSRs is important, and suggest that further guidance on how to use and include these data would help to promote their use in future systematic reviews. Most respondents who received CSRs considered them to be valuable in their systematic review and/or meta-analysis.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.