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Trial · NCT05216757

Registered outcomes16

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

ListOutcomeTime frameDescription
PrimaryChange from baseline in patient's assessment of arthritis pain on a visual analogue scale12 weeksChange from baseline in self-reported finger joint pain previous 48 hours on a 0-100 mm scale at 12 weeks of treatment; higher value indicate worse outcome.
SecondaryChange from baseline in patient's assessment of arthritis pain on a visual analogue scale prior to each visit4 weeks, 8 weeks, 12 weeksDifferences in self-reported finger joint pain previous 48 hours on a 0-100 mm scale at 4 weeks, 8 weeks, and 12 weeks; higher value indicate worse outcome.
SecondaryChange from baseline in Australian Canadian Hand Osteoarthritis Index (AUSCAN) scores at each visit.4 weeks, 8 weeks, 12 weeks
The AUSCAN Index is a self-administered questionnaire consisting of a 15-item scale which measures pain (5 items), stiffness (1 item) and degree of disability/physical function (9 items) during the preceding 48 hours; higher value indicate worse outcome.
SecondaryChange from baseline in Functional Index for Hand Osteoarthritis (FIHOA)12 weeksThe Functional Index for Hand Osteoarthritis (FIHOA) is a leading assessment tool for hand OA-related functional impairment; higher value indicate worse outcome.
SecondaryChange from baseline in Health Assessment Questionnaire Disability Index (HAQ)12 weeksChange from baseline in Health Assessment Questionnaire Disability Index (HAQ) at week 12; higher value indicate worse outcome.
SecondaryChange from baseline in the Scores of SF-36 questionnaire12 weeksChange from baseline in SF-36, including physical and mental component sores (PCS and MCS) at week 12; higher value indicate worse outcome.
SecondaryChange from baseline in Michigan Hand Outcomes Questionnaire (MHOQ)12 weeks
Michigan Hand Outcomes Questionnaire (MHOQ) pain and physical function subscales; function subscale range 10-50, higher value indicate worse outcome; task subscale range 17-85, higher value indicate worse outcome; work subscale range 5-25, higher value indicate worse outcome; pain subscale range 10-48, higher value indicate better outcome.
SecondaryChange from baseline in Ultrasound record12 weeksUltrasound record: number of finger joints with synovial thickening and power Doppler signals.
SecondaryChange from baseline in OMERACT hand OA magnetic resonance imaging score12 weeks
OMERACT hand OA magnetic resonance imaging score includes synovitis (0-3), erosive damage(0-3), cyst (0-3), osteophyte (0-3), cartilage space loss(0-3), malalignment (0-3), and bone marrow lesions (0-3); higher value indicate worse outcome
OtherChange from baseline in Erythrocyte Sedimentation Rate (ESR)12 weeksErythrocyte Sedimentation Rate (ESR); higher value indicate worse outcome.
OtherChange from baseline in C Reactive Protein (CRP)12 weeksC Reactive Protein (CRP); higher value indicate worse outcome.
OtherChange from baseline in patient's global assessment of disease activity on a visual analogue scale12 weeksChange from baseline in patient's global assessment of disease activity previous 48 hours on a 0-100 mm scale at 12 weeks of treatment; higher value indicate worse outcome.
OtherChange from baseline of physician's global assessment of disease activity on a visual analogue scale12 weeksChange from baseline in physician's global assessment of disease activity previous 48 hours on a 0-100 mm scale at 12 weeks of treatment; higher value indicate worse outcome.
OtherChange from baseline in Fingertip-to-palm distance12 weeksChange from baseline in Fingertip-to-palm distance, cm
OtherChange from baseline in grip strength12 weeksChange from baseline in grip strength, kg
OtherSwelling and Tender joint count, assessed by physician joint count12 weeksSwelling and Tender joint count, assessed by physician joint count

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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