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NuvaRing vs Combined Oral Contraceptives (COC): serious adverse events

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.03380.03120.0366wilsonClinicalTrials.gov
Risk in group 20.04410.04120.0473wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0104-0.0145-0.00626newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.7650.6880.851logClinicalTrials.gov
Odds ratio, group 1 over group 20.7570.6780.846logClinicalTrials.gov
Number needed to treat, for one fewer participant with a serious adverse event on NuvaRing than on Combined Oral Contraceptives (COC)96.569.1160from the risk difference intervalClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1NuvaRingUsers of an etonogestrel-containing and ethinylestradiol-containing vaginal ring57717,084EG000ClinicalTrials.gov
Group 2Combined Oral Contraceptives (COC)Users of combined oral contraceptive pills75117,016EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, serious adverse eventsClinicalTrials.gov
Time frameInformation on adverse events was collected over a period of 4 years.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleTransatlantic Active Surveillance on Cardiovascular Safety of NuvaRing (TASC)ClinicalTrials.gov
NCT numberNCT00524771ClinicalTrials.gov
PhasesClinicalTrials.gov
ConditionsContraceptionClinicalTrials.gov
InterventionsClinicalTrials.gov
Lead sponsorCenter for Epidemiology and Health Research, GermanyClinicalTrials.gov
Results first posted2014-04-09ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00524771?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.