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Trial · NCT06382987

Registered outcomes19

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

ListOutcomeTime frameDescription
PrimaryChange in percent Body Surface Area (BSA) involved affected by plaque psoriasis from baseline to follow up in participants treated with deucravacitinib.1 month, 3 months, 6 months and every 6 months up to 5 years
PrimaryNumber of participants who achieved Physician's Global Assessment (PGA) of 0/1 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
PrimaryNumber of participants who achieved Absolute Psoriasis Area and Severity Index (aPASI) of ≤2 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
PrimaryNumber of participants who achieved Dermatology Life Quality Index (DLQI) of 0 /1 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
PrimaryParticipant duration of treatment (time difference between date of treatment initiation to date of discontinuation)1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryChange in percent Body Surface Area (BSA) involved affected by plaque psoriasis from baseline to follow up in participants treated with deucravacitinib or apremilast1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieved Dermatology Life Quality Index (DLQI) of 0/1 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryParticipant duration of treatment (time difference between date of treatment initiation to date of discontinuation) from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants treated with deucravacitinib with a change in Physician's Global Assessment (PGA) from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants treated with deucravacitinib with a change in Dermatology Life Quality Index (DLQI) from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants achieving a Dermatology Life Quality Index (DLQI) score of ≤5 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve a Psoriasis Area Severity Index (PASI) response of 75 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve a Psoriasis Area Severity Index (PASI) response of 90 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve an absolute Psoriasis Area Severity Index (aPASI) score ≤5 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve an absolute Psoriasis Area Severity Index (aPASI) score ≤3 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve a National Psoriasis Foundation (NPF) Acceptable Body Surface Area response from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve an absolute scalp-specific Physician's Global Assessment (ss-PGA) of 0/1 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve an absolute Physician's Global Assessment-Fingernail (PGA-F) of 0/1 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years
SecondaryNumber of participants who achieve an absolute Palmoplantar Physician's Global Assessment (pp-PGA) of 0/1 from baseline to follow-up1 month, 3 months, 6 months and every 6 months up to 5 years

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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