Abstract Background Reporting of adverse events in randomized clinical trials (RCTs) is encouraged by the authors of The Consolidated Standards of Reporting Trials (CONSORT) statement. With robust methodological design and adequate reporting, RCTs have the potential to provide useful evidence on the incidence of adverse events associated with spinal manipulative therapy (SMT). During a previous investigation, it became apparent that comprehensive search strategies combining text words with indexing terms was not sufficiently sensitive for retrieving records that were known to contain reports on adverse events. The aim of this analysis was to compare the proportion of articles containing data on adverse events associated with SMT that were i...
Background Data suggest that certain psychological interventions can induce harm in a significant nu...
ObjectiveTo examine the degree of concordance in reporting serious adverse events (SAEs) from antide...
International audienceBackground: An accurate and comprehensive assessment of harms is a fundamental...
Background: We would expect information on adverse drug reactions in randomised clinical trials to b...
Objectives: To describe if there has been a change in the reporting of adverse events associated wit...
Background: We would expect information on adverse drug reactions in randomised clinical trials to ...
Systematic reviews should use search strategies which aim to identify as many relevant papers as pos...
Cornelius VR, Sauzet O, Williams JE, et al. Adverse event reporting in randomised controlled trials ...
Background: Adverse events (AEs) in clinical trials may be reported in multiple sources. Different m...
OBJECTIVE: To ascertain contemporary approaches to the collection, reporting and analysis of adverse...
BackgroundUnderreporting of harms in randomized controlled trials (RCTs) may lead to incomplete or e...
► structured review ► spine surgery ► disk replacement ► lumbar fusions ► adverse events Abstract St...
Phillips R, Hazell L, Sauzet O, Cornelius V. Analysis and reporting of adverse events in randomised ...
Objective: To determine (i) the difference in the frequency of serious adverse events (SAEs) reporte...
International audienceBACKGROUND: Reports of clinical trials usually emphasize efficacy results, esp...
Background Data suggest that certain psychological interventions can induce harm in a significant nu...
ObjectiveTo examine the degree of concordance in reporting serious adverse events (SAEs) from antide...
International audienceBackground: An accurate and comprehensive assessment of harms is a fundamental...
Background: We would expect information on adverse drug reactions in randomised clinical trials to b...
Objectives: To describe if there has been a change in the reporting of adverse events associated wit...
Background: We would expect information on adverse drug reactions in randomised clinical trials to ...
Systematic reviews should use search strategies which aim to identify as many relevant papers as pos...
Cornelius VR, Sauzet O, Williams JE, et al. Adverse event reporting in randomised controlled trials ...
Background: Adverse events (AEs) in clinical trials may be reported in multiple sources. Different m...
OBJECTIVE: To ascertain contemporary approaches to the collection, reporting and analysis of adverse...
BackgroundUnderreporting of harms in randomized controlled trials (RCTs) may lead to incomplete or e...
► structured review ► spine surgery ► disk replacement ► lumbar fusions ► adverse events Abstract St...
Phillips R, Hazell L, Sauzet O, Cornelius V. Analysis and reporting of adverse events in randomised ...
Objective: To determine (i) the difference in the frequency of serious adverse events (SAEs) reporte...
International audienceBACKGROUND: Reports of clinical trials usually emphasize efficacy results, esp...
Background Data suggest that certain psychological interventions can induce harm in a significant nu...
ObjectiveTo examine the degree of concordance in reporting serious adverse events (SAEs) from antide...
International audienceBackground: An accurate and comprehensive assessment of harms is a fundamental...