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Comparison · NCT03129321-6cc3e7ca

Test vs Reference Standard: Proportion of Patients in Each Active Treatment Group Who Are Considered a Mycological Cure

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. Test vs Reference Standard: Proportion of Patients in Each Active Treatment Group Who Are Considered a Mycological Cure. Trial comparisons, record NCT03129321-6cc3e7ca. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03129321-6cc3e7ca

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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 10.7350.6670.793wilson
Risk in group 20.7350.6640.796wilson
Risk difference, group 1 minus group 2-0.000159-0.09120.0917newcombe hybrid score
Risk ratio, group 1 over group 210.8821.13log
Odds ratio, group 1 over group 20.9990.6231.6log
Number needed to treat, for one fewer participant with the outcome on Test than on Reference Standard6,290from 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 1TestEconazole Nitrate Cream, 1%, topical, sufficient amount to cover all affected areas on the feet once daily for 28 days~Econazole Nitrate Cream, 1%136185OG000
Group 2Reference StandardEconazole Nitrate Cream, 1%, topical, sufficient amount to cover all affected areas on the feet once daily for 28 days~Econazole Nitrate Cream, 1%125170OG001

Outcome

Type
SECONDARY
Title
Proportion of Patients in Each Active Treatment Group Who Are Considered a Mycological Cure
Description
To be considered a mycological cure the patient must have a negative KOH test and a negative fungal culture for T. rubrum, T. mentagrophytes or E. floccosum
Time frame
Day 42
Population
Active treatment groups of the Per Protocol population

Source ClinicalTrials.gov

Trial

Title
Therapeutic Equivalence and Safety of Two Econazole Nitrate Cream, 1% Products in Tinea Pedis
NCT number
NCT03129321
Phases
PHASE3
Conditions
Tinea Pedis
Interventions
Econazole Nitrate Cream, 1%, Placebo
Lead sponsor
Mylan Inc.
Results first posted
2018-08-02

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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