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Trial · NCT02097264

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryChange in the total histopathological synovitis scoreWeek 0, week 12
SecondaryChange in dynamic contrast enhanced MRI (DCE-MRI) measures of initial rate of enhancement (IRE)Week 0, week 12
SecondaryChange in dynamic contrast enhanced MRI (DCE-MRI) measures of maximal enhancement (ME)Week 0, week 12
SecondaryChanges in RA-MRI scores (RAMRIS (Rheumatoid arthritis magnetic resonance imaging)) of synovitisWeek 0, week 12
SecondaryChanges in RA-MRI scores (RAMRIS) of oedemaWeek 0, week 12
SecondaryChanges in RA-MRI scores (RAMRIS) of erosionWeek 0, week 12
SecondaryChange in high frequency ultrasound with Power Doppler measures of total synovitisWeek 0, week 12
SecondaryChange in high frequency ultrasound with Power Doppler measures of total tenosynovitis scoresWeek 0, week 12
SecondaryChange in disease activity 28 - C-reactive protein (DAS28 (CRP)Week 0, week 12
SecondaryIncidence of Adverse Events (AE)Week 0, week 24
SecondaryIncidence of local intolerability at the injection siteWeek 0, week 24

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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