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Comparison · NCT00074412-sae

Nevirapine vs Placebo: 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. Nevirapine vs Placebo: serious adverse events. Trial comparisons, record NCT00074412-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00074412-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 10.2010.1740.231wilson
Risk in group 20.1850.1590.214wilson
Risk difference, group 1 minus group 20.0152-0.02450.0549newcombe hybrid score
Risk ratio, group 1 over group 21.080.8811.33log
Odds ratio, group 1 over group 21.10.8551.42log
Number needed to harm, for one more participant with a serious adverse event on Nevirapine than on Placebo65.6from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1NevirapineFor infants: extended treatment with NVP152758EG000
Group 2PlaceboFor infants: extended treatment with NVP placebo141761EG001

Harm

What it counts
Total, serious adverse events
Time frame
Regardless of seriousness, severity or relatedness all AEs occurring in infants after enrollment (birth) and throughout the duration of the study (18 months) must be recorded.

Source ClinicalTrials.gov

Trial

Title
Using Nevirapine to Prevent Mother-to-Child HIV Transmission During Breastfeeding
NCT number
NCT00074412
Phases
PHASE3
Conditions
HIV Infections
Interventions
Nevirapine, Nevirapine placebo
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Results first posted
2013-09-16

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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