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Comparison · NCT02301390-sae

Amiodarone Only vs Amiodarone + Catheter Ablation: 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. Amiodarone Only vs Amiodarone + Catheter Ablation: serious adverse events. Trial comparisons, record NCT02301390-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02301390-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 10.4070.2450.593wilson
Risk in group 20.3080.1650.5wilson
Risk difference, group 1 minus group 20.0997-0.1520.334newcombe hybrid score
Risk ratio, group 1 over group 21.320.6352.76log
Odds ratio, group 1 over group 21.550.4984.8log
Number needed to harm, for one more participant with a serious adverse event on Amiodarone Only than on Amiodarone + Catheter Ablation10from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Amiodarone OnlyAmiodarone is a Class III antiarrhythmic agent.1127EG000
Group 2Amiodarone + Catheter AblationAmiodarone is a Class III antiarrhythmic agent.~Catheter VT Ablation: The ablation procedure uses radiofrequency energy to destroy cardiac tissue at the origin of the arrhythmia.826EG001

Harm

What it counts
Total, serious adverse events
Time frame
24 months

Source ClinicalTrials.gov

Trial

Title
INTERVENE: Indian Trial of Endocardial Ventricular Substrate Ablation to Prevent Recurrent VT Events
NCT number
NCT02301390
Phases
NA
Conditions
Ventricular Tachycardia
Interventions
Amiodarone, Catheter Ablation
Lead sponsor
Icahn School of Medicine at Mount Sinai
Results first posted
2020-01-27

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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