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Comparison · NCT00274261-sae

C31G vs Conceptrol: 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. C31G vs Conceptrol: serious adverse events. Trial comparisons, record NCT00274261-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00274261-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 10.0120.006510.0219wilson
Risk in group 20.02140.01230.0371wilson
Risk difference, group 1 minus group 2-0.00947-0.0260.00401newcombe hybrid score
Risk ratio, group 1 over group 20.5580.2431.28log
Odds ratio, group 1 over group 20.5530.2371.29log
Number needed to treat, for one fewer participant with a serious adverse event on C31G than on Conceptrol106from 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 1C31GC31G vaginal gel contains 35mg (1% concentration) of C31G in 3.5 mL volume of gel10836EG000
Group 2ConceptrolConceptrol® Vaginal gel contains 100mg (4% concentration) of nonoxynol-9 (N-9) in 2.5mL volume of gel.12560EG001

Harm

What it counts
Total, serious adverse events
Time frame

Source ClinicalTrials.gov

Trial

Title
Study of the Safety and Contraceptive Efficacy of C31G Compared to Conceptrol®
NCT number
NCT00274261
Phases
PHASE3
Conditions
Pregnancy
Interventions
C31G, nonoxynol-9 (N-9)
Lead sponsor
Premier Research
Results first posted
2013-06-06

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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