SynthesisBMC medical research methodology2018
A systematic review of comparisons between protocols or registrations and full reports in primary biomedical research.
Synthesis in BMC medical research methodology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 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
25 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Estimating the prevalence of discrepancies between study registrations and publications: a systematic review and meta-analyses.BMJ open · 2023Pooled it
- Closing the gap between systematic review protocols and publication in anesthesiology: shared responsibility for transparency and accountability.Canadian journal of anaesthesia = Journal canadien d'anesthesie · 2026Article
- Outcome switching in cohort studies of interventions: meta-epidemiological study.BMJ (Clinical research ed.) · 2026Article
- Consistency Between Clinical Trial Registry Entries and Journal Publications in Transfusion Medicine: An Observational Study.Journal of clinical medicine · 2026Article
- An investigation of discrepancies in outcome reporting and selective reporting bias in interrupted time series studies of health interventions: a methodological study.BMC public health · 2026Article
- [Methodological and ethical congruence in medical research protocols at a local hospital committee].Revista medica del Instituto Mexicano del Seguro Social · 2026Observational
- Misreporting of Patient-Relevant and Study Design Elements in Anesthesiology Randomized Controlled Trials: An Observational Study.Medical sciences (Basel, Switzerland) · 2025Observational
- What happens to qualitative studies initially presented as conference abstracts: A survey among study authors.Research synthesis methods · 2025Article
- Exploring ethical elements in reporting guidelines: results from a research-on-research study.Research integrity and peer review · 2025Article
- Exploring open science practices in behavioural public policy research.Royal Society open science · 2024Article
- Dissemination of Registered COVID-19 Clinical Trials (DIRECCT): a cross-sectional study.BMC medicine · 2023Article
- Reasons for missing evidence in rehabilitation meta-analyses: a cross-sectional meta-research study.BMC medical research methodology · 2023Article
- Completeness and consistency of primary outcome reporting in COVID-19 publications in the early pandemic phase: a descriptive study.BMC medical research methodology · 2023Article
- Registered report: Survey on attitudes and experiences regarding preregistration in psychological research.PloS one · 2023Article
- Changes to design and analysis elements of research plans during randomised controlled trials in Australia.The Medical journal of Australia · 2022Article
- Quality Output Checklist and Content Assessment (QuOCCA): a new tool for assessing research quality and reproducibility.BMJ open · 2022Review
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- Ten simple rules for good research practice.PLoS computational biology · 2022Article
- Subgroup Analysis in Pulmonary Hypertension-Specific Therapy Clinical Trials: A Systematic Review.Journal of personalized medicine · 2022Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
21 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundProspective study protocols and registrations can play a significant role in reducing incomplete or selective reporting of primary biomedical research, because they are pre-specified blueprints which are available for the evaluation of, and comparison with, full reports. However, inconsistencies between protocols or registrations and full reports have been frequently documented. In this systematic review, which forms part of our series on the state of reporting of primary biomedical, we aimed to survey the existing evidence of inconsistencies between protocols or registrations (i.e., what was planned to be done and/or what was actually done) and full reports (i.e., what was reported in the literature); this was based on findings from systematic reviews and surveys in the literature.
methodsElectronic databases, including CINAHL, MEDLINE, Web of Science, and EMBASE, were searched to identify eligible surveys and systematic reviews. Our primary outcome was the level of inconsistency (expressed as a percentage, with higher percentages indicating greater inconsistency) between protocols or registration and full reports. We summarized the findings from the included systematic reviews and surveys qualitatively.
resultsThere were 37 studies (33 surveys and 4 systematic reviews) included in our analyses. Most studies (n = 36) compared protocols or registrations with full reports in clinical trials, while a single survey focused on primary studies of clinical trials and observational research. High inconsistency levels were found in outcome reporting (ranging from 14% to 100%), subgroup reporting (from 12% to 100%), statistical analyses (from 9% to 47%), and other measure comparisons. Some factors, such as outcomes with significant results, sponsorship, type of outcome and disease speciality were reported to be significantly related to inconsistent reporting.
conclusionsWe found that inconsistent reporting between protocols or registrations and full reports of primary biomedical research is frequent, prevalent and suboptimal. We also identified methodological issues such as the need for consensus on measuring inconsistency across sources for trial reports, and more studies evaluating transparency and reproducibility in reporting all aspects of study design and analysis. A joint effort involving authors, journals, sponsors, regulators and research ethics committees is required to solve this problem.
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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.