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Users of DRSP vs Users of LNG: Number of Participants With Venous Thromboembolism (VTE)

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 10.001570.001070.0023wilsonClinicalTrials.gov
Risk in group 20.001620.00110.00239wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0000479-0.0009660.00085newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.970.5611.68logClinicalTrials.gov
Odds ratio, group 1 over group 20.970.561.68logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Users of DRSP than on Users of LNG20,900from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Users of DRSPWomen who use authorized oral contraceptives containing DRSP prescribed by their gynecologist2616,534OG000ClinicalTrials.gov
Group 2Users of LNGWomen who use authorized oral contraceptives containing LNG prescribed by their gynecologist2515,428OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleNumber of Participants With Venous Thromboembolism (VTE)ClinicalTrials.gov
DescriptionClinicalTrials.gov
Time frame1.5 to 5 yearsClinicalTrials.gov
Population
The primary analysis compares the users of DRSP and LNG. Its results are presented below. The comparison of users of DRSP and OCs containing other progestins was only conducted for exploratory reasons. This secondary analysis showed similar results and is described in more detail in the publication of study results, see citations.
ClinicalTrials.gov

Trial 8

FieldValueSource
TitleEuropean Active Surveillance Study (EURAS)ClinicalTrials.gov
NCT numberNCT00302848ClinicalTrials.gov
PhasesClinicalTrials.gov
ConditionsContraceptionClinicalTrials.gov
InterventionsDrospirenone, Levonorgestrel, Other progestin containing oral contraceptiveClinicalTrials.gov
Lead sponsorCenter for Epidemiology and Health Research, GermanyClinicalTrials.gov
Results first posted2009-11-20ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00302848?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.