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Trial · NCT04042857

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMycological Cure at 48 WeeksBaseline to 48 WeeksMycological cure rate at week 48 as defined by negative potassium hydroxide examination and negative culture of the target hallux nail
PrimaryClinical Efficacy at 48 WeeksBaseline to 48 WeeksClinical efficacy rate at week 48 as defined by less than 10% clinical involvement of the target hallux nail
SecondaryComplete Cure at Week 48Baseline to 48 WeeksComplete cure rate at week 48 defined as 0% clinical involvement, negative potassium hydroxide examination and negative culture of the target hallux nail
SecondaryComplete Cure at Week 52Baseline to 52 WeeksComplete cure rate at week 52 defined as 0% clinical involvement, negative mycology, and negative potassium hydroxide examination of the target hallux nail at week 52
SecondaryAlmost Complete Cure at Week 48Baseline to 48 WeeksAlmost complete cure rate at week 48 defined as less than 10% clinical involvement, negative potassium hydroxide examination, and negative culture of the target hallux nail at week 48
SecondaryAlmost Complete Cure at Week 52Baseline to Week 52Almost complete cure rate at week 52 defined as less than 10% clinical involvement, negative potassium hydroxide examination, and negative culture of the target hallux nail at Week 52
SecondaryTime to Complete CureBaseline to 52 WeeksMeasured across all observation points
SecondaryTime to Almost Complete CureBaseline to 52 WeeksMeasured across all observation points
SecondaryPercent Change in Area of Nail InvolvementBaseline to 52 WeeksCalculated as a ratio of clear to involved measured across all observation points
SecondaryGrowth of Clear NailBaseline to 52 WeeksChange in area of clear nail growth measured across all observation points
SecondaryMycological Cure RateBaseline to 52 Weeks
Changes in mycological cure rates (Changes in the proportion of subjects who achieved mycological cure, defined as negative culture and potassium hydroxide examination) measured across all observation points
SecondaryDermatopyhyte Identification and CharacterizationBaseline to 52 WeeksChanges in the types of dermatophytes dermatophytes across all observation points
SecondaryOverall Fungal SpeciesBaseline to 52 WeeksChange types of overall fungal species across all observation points

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

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GET https://conductscience.org/api/trials/v1/NCT04042857/registered