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Trial · NCT07335588

Registered outcomes19

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants Achieving IGA-LS TS at Week 12Week 12
SecondaryNumber of Participants Achieving IGA-LS TS at Week 8Week 8
SecondaryChange in Clinical Lichen Sclerosus Score (CLISSCO) from Baseline to Week 12Baseline to Week 12
SecondaryNumber of Participants Achieving a Reduction of Skin Pain Numerical Rating Scale (NRS) Score (Weekly Average) of ≥4 Points from Baseline to Week 12 in Participants with Baseline Skin Pain NRS Score ≥4Baseline to Week 12
SecondaryNumber of Participants Achieving a Reduction of Skin Pain NRS Score (Weekly Average) of ≥4 Points from Baseline to Week 8 in Participants with Baseline Skin Pain NRS Score ≥4Baseline to Week 8
SecondaryNumber of Participants Achieving a Reduction of Itch NRS Score (Weekly Average) of ≥4 Points from Baseline to Week 12 in Participants with Baseline Itch NRS Score ≥4Baseline to Week 12
SecondaryNumber of Participants Achieving a Reduction of Itch NRS Score (Weekly Average) of ≥4 Points from Baseline to Week 8 in Participants with Baseline Itch NRS Score ≥4Baseline to Week 8
SecondaryChange in Vulvar Quality of Life Index (VQLI) Score from Baseline to Week 12Baseline to Week 12
SecondaryNumber of Participants Achieving IGA-LS TS at Week 52Week 52
SecondaryChange in CLISSCO Score from Baseline to Week 52Baseline to Week 52
SecondaryNumber of Participants Achieving IGA-LS TS at Week 52 Among Participants Having Achieved IGA-LS TS at Week 12Week 52
SecondaryNumber of Participants Achieving an IGA-LS Score of 0 or 1 at Week 52 Among Participants Having Achieved IGA-LS TS at Week 12Week 52
SecondaryTime to IGA-LS TS from Baseline to Week 52Baseline to Week 52
SecondaryTime to IGA-LS ≥2 from Week 12 to Week 52 Among Participants Having Achieved IGA-LS TS at Week 12Week 12 to Week 52
SecondaryNumber of Participants Having no Increase in CLISSCO Architectural Changes Domain Score from Baseline to Week 52Baseline to Week 52
SecondaryNumber of Participants Achieving a Reduction of Skin Pain NRS Score (Weekly Average) of ≥4 Points from Baseline to Week 52 in Participants with Baseline Skin Pain NRS Score ≥4Baseline to Week 52
SecondaryNumber of Participants Achieving a Reduction of Itch NRS Score (Weekly Average) of ≥4 Points from Baseline to Week 52 in Participants with Baseline Itch NRS Score ≥4Baseline to Week 52
SecondaryNumber of Treatment-emergent Adverse Events (TEAEs) from Baseline to Week 12Baseline to Week 12
SecondaryNumber of TEAEs from Week 12 to Week 54Week 12 to Week 54

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.

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GET https://conductscience.org/api/trials/v1/NCT07335588/registered