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Comparison · NCT03637660-sae

One Dose BPG 2.4 MU vs Three Doses BPG 2.4 MU: 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. One Dose BPG 2.4 MU vs Three Doses BPG 2.4 MU: serious adverse events. Trial comparisons, record NCT03637660-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03637660-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 10.008060.001430.0443wilson
Risk in group 20.0160.00440.0565wilson
Risk difference, group 1 minus group 2-0.00794-0.04890.0301newcombe hybrid score
Risk ratio, group 1 over group 20.5040.04635.49log
Odds ratio, group 1 over group 20.50.04485.59log
Number needed to treat, for one fewer participant with a serious adverse event on One Dose BPG 2.4 MU than on Three Doses BPG 2.4 MU126from 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 1One Dose BPG 2.4 MU2.4 MU of BPG intramuscularly on Day 11124EG000
Group 2Three Doses BPG 2.4 MU2.4 MU of BPG intramuscularly weekly for three successive weeks2125EG001

Harm

What it counts
Total, serious adverse events
Time frame
Day 1 through Day 31

Source ClinicalTrials.gov

Trial

Title
Phase 4 Comparative Trial of Benzathine Penicillin G for Treatment of Early Syphilis in Subjects With or Without HIV Infection
NCT number
NCT03637660
Phases
PHASE4
Conditions
Syphilis
Interventions
Benzathine Penicillin
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Results first posted
2023-12-26

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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