MedPath

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 patients
Rheumatoid 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
NameTimeMethod
DAS-28 score 8 weeks Composite end point
Secondary Outcome Measures
NameTimeMethod
ACR 20 8 weeks Composite endpoint
© Copyright 2025. All Rights Reserved by MedPath