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Comparison · NCT00667368-sae

Intervention vs Control: 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. Intervention vs Control: serious adverse events. Trial comparisons, record NCT00667368-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00667368-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 10.01020.004970.021wilson
Risk in group 20.00440.00150.0129wilson
Risk difference, group 1 minus group 20.00585-0.004110.017newcombe hybrid score
Risk ratio, group 1 over group 22.330.6058.97log
Odds ratio, group 1 over group 22.340.6049.1log
Number needed to harm, for one more participant with a serious adverse event on Intervention than on Control171from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Intervention
Metronidazole 500mg twice daily for 7 days for Bacterial Vaginosis (BV) detection~Metronidazole: Bi-monthly testing and treatment for BV with Metronidazole if BV is detected; 500mg twice daily for 7 days.
7683EG001
Group 2ControlBi-monthly testing for BV without treatment.3682EG000

Harm

What it counts
Total, serious adverse events
Time frame
12 months after enrollment

Source ClinicalTrials.gov

Trial

Title
Bacterial Vaginosis Home Screening to Prevent STDs
NCT number
NCT00667368
Phases
PHASE3
Conditions
Bacterial Vaginosis
Interventions
Metronidazole
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Results first posted
2015-10-29

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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