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Trial · NCT06622603

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryThe proportion of patients with serum urate levels <7.0 mg/dL6 monthsThe proportion of patients who maintain serum urate levels \<7.0 mg/dL at 6 months after taking febuxostat 20 mg once daily or after suspending urate-lowering agents
SecondaryThe proportion of subjects with serum urate <7.0 mg/dL6 months and 12 monthsWe will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months
SecondarySerum urate levels6 months and 12 monthsWe will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months
SecondaryGout Impact Scale (GIS) score using the Korean version6 months and 12 monthsWe will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months
SecondaryPatient's overall assessment of gout using a visual analog scale6 months and 12 monthsWe will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months
SecondaryEuroQol(EQ)-5D score6 months and 12 monthsWe will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months
SecondaryGout activity score (GAS)6 months and 12 months
GAS is calculated as (0.09 × last 12-month attacks) + \[1.01 × square root (serum uric acid)\] + \[0.34 × VAS patient\] + \[0.53 × ln (1 + tophi number)\] We will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months.
SecondaryDrug adherence6 months and 12 months
Adherence is defined as defined as taking 80% or more of the prescribed medication (using by the number of remaining pills). We will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months.
SecondaryIncidence rate of acute gouty arthritis6 months and 12 monthsWe will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months.
SecondarySwollen and tender joint counts of 66/68 joints6 months and 12 monthsWe will compare among maintaining, reducing, and discontinuing groups at 6 months and between maintaining and reducing groups at 12 months.
OtherThe reliability of the ultrasound scoring system for tophi in gout patientsBaselineWe will compare the USG scores evaluated by each institution with ones evaluated by an independent review committee.

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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