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Comparison · NCT01617096-sae

Dapivirine Vaginal Ring vs Placebo Ring: 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. Dapivirine Vaginal Ring vs Placebo Ring: serious adverse events. Trial comparisons, record NCT01617096-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01617096-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 10.08830.07420.105wilson
Risk in group 20.09880.08380.116wilson
Risk difference, group 1 minus group 2-0.0104-0.03280.0119newcombe hybrid score
Risk ratio, group 1 over group 20.8940.7051.14log
Odds ratio, group 1 over group 20.8840.681.15log
Number needed to treat, for one fewer participant with a serious adverse event on Dapivirine Vaginal Ring than on Placebo Ring95.8from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Dapivirine Vaginal RingVaginal ring containing 25mg dapivirine~Dapivirine Vaginal Ring: Dosage form: vaginal ring Dosage: 25mg Frequency: monthly Duration: 12 months1161,313EG000
Group 2Placebo RingVaginal ring containing no drug substance~Placebo Ring: Vaginal ring containing no drug substance1301,316EG001

Harm

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

Source ClinicalTrials.gov

Trial

Title
Phase 3 Safety and Effectiveness Trial of Dapivirine Vaginal Ring for Prevention of HIV-1 in Women
NCT number
NCT01617096
Phases
PHASE3
Conditions
HIV Infections
Interventions
Dapivirine Vaginal Ring, Placebo Ring
Lead sponsor
International Partnership for Microbicides, Inc.
Results first posted
2022-12-16

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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