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Comparison · NCT03017846-4b11824c

Current Study vs NCT02665260: Number of Patients Achieving Complete Lesion Clearance Compared to Prior Study (NCT02665260)

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. Current Study vs NCT02665260: Number of Patients Achieving Complete Lesion Clearance Compared to Prior Study (NCT02665260). Trial comparisons, record NCT03017846-4b11824c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03017846-4b11824c

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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 10.440.2670.629wilson
Risk in group 20.3040.1560.509wilson
Risk difference, group 1 minus group 20.136-0.1320.376newcombe hybrid score
Risk ratio, group 1 over group 21.450.6763.09log
Odds ratio, group 1 over group 21.80.5475.89log
Number needed to treat, for one more participant with the outcome on Current Study than on NCT026652607.37from 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 1Current StudySubjects with lesions treated with topical cantharidin every 3 weeks up to 12 weeks in the present study.~Cantharidin: Application of topical cantharidin1125OG000
Group 2NCT02665260Subjects with lesions treated with topical cantharidin every 3 weeks up to 12 weeks in the previous study NCT02665260.~Cantharidin: Application of topical cantharidin723OG001

Outcome

Type
SECONDARY
Title
Number of Patients Achieving Complete Lesion Clearance Compared to Prior Study (NCT02665260)
Description
Comparison of the number of subjects achieving complete lesion clearance at study completion (up to 12 weeks) to the same measure obtained in our previous study (NCT02665260)
Time frame
At study completion, up to 12 weeks
Population

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy of Topical Cantharidin for the Treatment of Molluscum Contagiosum, Phase 2
NCT number
NCT03017846
Phases
PHASE2
Conditions
Molluscum Contagiosum
Interventions
Cantharidin
Lead sponsor
Steven R Cohen
Results first posted
2019-01-30

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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