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Comparison · NCT03176953-sae

Prolonged Exposure + Topiramate vs Prolonged Exposure + 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. Prolonged Exposure + Topiramate vs Prolonged Exposure + Placebo: serious adverse events. Trial comparisons, record NCT03176953-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03176953-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 10.060.02060.162wilson
Risk in group 20.040.0110.135wilson
Risk difference, group 1 minus group 20.02-0.08250.126newcombe hybrid score
Risk ratio, group 1 over group 21.50.2628.6log
Odds ratio, group 1 over group 21.530.2459.59log
Number needed to harm, for one more participant with a serious adverse event on Prolonged Exposure + Topiramate than on Prolonged Exposure + Placebo50from 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 1Prolonged Exposure + Topiramatepsychotherapy plus active medication~topiramate: active medication~prolonged exposure: psychotherapy350EG000
Group 2Prolonged Exposure + Placebopsychotherapy plus placebo medication~prolonged exposure: psychotherapy~placebo: non-active medication250EG001

Harm

What it counts
Total, serious adverse events
Time frame
Duration of study participation - 10 months

Source ClinicalTrials.gov

Trial

Title
Topiramate and Prolonged Exposure
NCT number
NCT03176953
Phases
PHASE2, PHASE3
Conditions
PTSD and Alcohol Use Disorder
Interventions
topiramate, prolonged exposure, placebo
Lead sponsor
VA Office of Research and Development
Results first posted
2023-11-18

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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