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Trial · NCT06965244

Registered outcomes13

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

ListOutcomeTime frameDescription
PrimaryProportion of patients who achieve decrease of at least 50% from baseline in the CLASI activity (CLASI-A) scoreAt week 16CLASI : Cutaneous LE disease Area and Severity Index
SecondaryPercentage of patients reaching CLASI-A 70At week 16CLASI : Cutaneous LE disease Area and Severity Index
SecondaryProportion of participants who achieve complete or almost complete response (CLASI-A 0-3)At week 16CLASI : Cutaneous LE disease Area and Severity Index
SecondaryPercentage of patients reaching CLASI-A 70At week 24CLASI : Cutaneous LE disease Area and Severity Index
SecondaryProportion of participants who achieve complete or almost complete response (CLASI-A 0-3)At week 24CLASI : Cutaneous LE disease Area and Severity Index
SecondaryVariation of Quality of life using DLQIAt week 16DLQI : Dermatology Life Quality Index
SecondaryVariation of Quality of life using DLQIAt week 24DLQI : Dermatology Life Quality Index
SecondarySLE activity using SLEDAIUp to 24 weeksSLEDAI : Systemic Lupus Erythematosus Disease Activity Index
SecondarySLE flare using SENELA-SLEDAI Flare Index (SFI)Up to 24 weeksSELENA : Safety of Estrogens in Lupus Erythematosus National Assessment SLEDAI : Systemic Lupus Erythematosus Disease Activity Index
SecondaryVariation of GCs doseBetween inclusion and week 24.
SecondaryVariation of damage in each group using CLASI-DAt week 24CLASI : Cutaneous LE disease Area and Severity Index
SecondaryVariation of damage in each group using CLASI-DAt week 16CLASI : Cutaneous LE disease Area and Severity Index
SecondaryRate of adverse eventsUp to 24 weeks

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/NCT06965244/registered