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Comparison · NCT01135017-sae

Dronedarone vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Dronedarone vs Placebo: serious adverse events. Trial comparisons, record NCT01135017-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01135017-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1230.06080.232wilson
Risk in group 20.1270.0630.24wilson
Risk difference, group 1 minus group 2-0.00447-0.1330.123newcombe hybrid score
Risk ratio, group 1 over group 20.9650.3622.57log
Odds ratio, group 1 over group 20.960.3132.94log
Number needed to treat, for one fewer participant with a serious adverse event on Dronedarone than on Placebo224from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1DronedaroneDronedarone 400 mg twice a day for 12 weeks757EG001
Group 2PlaceboPlacebo (for dronedarone) twice a day for 12 weeks755EG000

Harm

What it counts
Total, serious adverse events
Time frame
All Adverse Events (AE) were collected regardless of seriousness or relationship to the drug in the period spanning from signature of the Informed Consent Form up to the last visit.

Source ClinicalTrials.gov

Trial

Title
Effects of Dronedarone on Atrial Fibrillation Burden in Subjects With Permanent Pacemakers
NCT number
NCT01135017
Phases
PHASE4
Conditions
Atrial Fibrillation
Interventions
Dronedarone, Placebo (for Dronedarone)
Lead sponsor
Sanofi
Results first posted
2013-04-01

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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