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Adverse event assessment, analysis, and reporting in recent published analgesic clinical trials: ACTTION systematic review and recommendations

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References

2003Core outcome domains for chronic pain clinical trials: IMMPACT recommendations3,496 cited
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2010The quality of safety reporting in trials is still suboptimal: Survey of major general medical journals84 cited
2012Adherence to CONSORT harms-reporting recommendations in publications of recent analgesic clinical trials: An ACTTION systematic review65 cited

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2015Adverse event methods were heterogeneous and insufficiently reported in randomized trials on persistent depressive disorder45 cited
2017Checklist for the preparation and review of pain clinical trial publications: a pain-specific supplement to CONSORT45 cited
2014Adverse event reporting in nonpharmacologic, noninterventional pain clinical trials: ACTTION systematic review27 cited
2019Recommendations for the Reporting of Harms in Manuscripts on Clinical Trials Assessing Osteoarthritis Drugs: A Consensus Statement from the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO)

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20 cited

2016Adverse Event Reporting in Clinical Trials of Intravenous and Invasive Pain Treatments: An ACTTION Systematic Review19 cited

2015Assessment of the quality of harms reporting in non-randomised studies and randomised controlled studies of topiramate for the treatment of epilepsy using CONSORT criteria15 cited

2020Adherence to Consolidated Standards of Reporting Trials (CONSORT) Guidelines for Reporting Safety Outcomes in Trials of Medical Cannabis and Cannabis-based Medicines for Chronic Noncancer Pain14 cited