A randomized double-blind controlled trial to assess the efficacy and safety of curcumin versus placebo in active rheumatoid arthritis patients
Phase 4
Recruiting
- Conditions
- Active rheumatoid arthritis patientsRheumatoid arthritis
- Registration Number
- TCTR20181115012
- Lead Sponsor
- Rheumatic Disease Unit, Department of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 34
Inclusion Criteria
RA (2010 ACR/EULAR criteria)
Age ≥ 18 years old
At least moderate disease activity (DAS 28 >3.2)
VAS ≥ 50
Stable dose DMARDs therapy at least 1 month prior to randomization
Inaccessible or denied add on therapy
Exclusion Criteria
Allergy to tumeric
Pregnant or breast feeding
Subjects with any current malignancy and on chemotherapy
On anticoagulant
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method DAS-28 score 8 weeks Composite end point
- Secondary Outcome Measures
Name Time Method ACR 20 8 weeks Composite endpoint