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Comparison · NCT01790659-sae

WR 279,396 vs Paromomycin: 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. WR 279,396 vs Paromomycin: serious adverse events. Trial comparisons, record NCT01790659-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01790659-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 10.009950.002730.0355wilson
Risk in group 20.005050.0008920.028wilson
Risk difference, group 1 minus group 20.0049-0.01920.0308newcombe hybrid score
Risk ratio, group 1 over group 21.970.1821.6log
Odds ratio, group 1 over group 21.980.17822log
Number needed to harm, for one more participant with a serious adverse event on WR 279,396 than on Paromomycin204from 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 1WR 279,396(Paromomycin and Gentamicin Topical Cream)~WR 279,396: WR 279,396 is a topical cream of paromomycin 15% and gentamicin 0.5%2201EG000
Group 2ParomomycinParomomycin alone~Paromomycin: Paromomycin alone1198EG001

Harm

What it counts
Total, serious adverse events
Time frame
AE's were assessed at baseline, days 2-9 daily, day 20, 35, 49, 63, 100, and 168 (applicable)

Source ClinicalTrials.gov

Trial

Title
Phase 3 Study of Walter Reed (WR) 279,396 and Paromomycin Alone for the Treatment of Cutaneous Leishmaniasis in Panama
NCT number
NCT01790659
Phases
PHASE3
Conditions
Cutaneous Leishmaniasis
Interventions
WR 279,396, Paromomycin
Lead sponsor
U.S. Army Medical Research and Development Command
Results first posted
2017-08-23

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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