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Clinical Trials/NCT03017118
NCT03017118
Recruiting
Not Applicable

A Randomized Controlled Trial Using Turmeric for Patients With Basal Joint Arthritis

Massachusetts General Hospital1 site in 1 country60 target enrollmentAugust 9, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Thumb Osteoarthritis
Sponsor
Massachusetts General Hospital
Enrollment
60
Locations
1
Primary Endpoint
Change in baseline pain intensity
Status
Recruiting
Last Updated
5 months ago

Overview

Brief Summary

The aim of this study is to assess whether the use of a commercially available nutraceutical, turmeric, is an effective option to manage pain and stiffness in patients with basal joint arthritis. To conduct a pilot Randomized Controlled Trial evaluating the impact of turmeric on basal joint arthritis.

Registry
clinicaltrials.gov
Start Date
August 9, 2017
End Date
January 1, 2028
Last Updated
5 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Neal Chung-Jen Chen

Medical Doctor

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • 40 years of age or older
  • English fluency and literacy
  • Seeking care for basal joint pain
  • Tender over basal joint
  • Positive distraction rotation test (rotation of the thumb metacarpal base while applying axial traction)
  • Radiographic evidence of Eaton stage 1 and 2 only

Exclusion Criteria

  • Secondary gains (litigations or worker compensation) procedures that may interfere with patients' motivation for treatment
  • Inability or unwillingness to participate in a trial study
  • Rheumatoid Arthritis or other inflammatory disorder diagnoses
  • Post-traumatic osteoarthritis
  • Patients on Coumadin/Steroids/NSAIDs/Tylenol
  • Diabetes Mellitus
  • Pregnant or lactating women
  • Basal joint arthritis of Eaton stage 3
  • Patients seeking other treatment for their basal joint arthritis (splint, corticosteroid injection, surgery)

Outcomes

Primary Outcomes

Change in baseline pain intensity

Time Frame: Enrollment, 6 weeks, and 3 months

0-10 ordinal rating of pain intensity

Change in baseline disability

Time Frame: Enrollment, 6 weeks, and 3 months

Disability measured by the QuickDASH

Study Sites (1)

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