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Effect of Unani Formulation and ibubrofen in the treatment of Osteoarthritis

Phase 2
Recruiting
Registration Number
CTRI/2010/091/000585
Lead Sponsor
Central council for research in Unani medicine-CCRUM
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Aged between 40 to 70 years
Either Sex
Patients diagnosed according to American College of Rheumatology Criteria for osteoarthritis of different joints will be selected
Patients with symptoms consistent with osteoarthritis of the joint involved for at least six months prior to screening.
Patients, who will be willing to discontinue all NSAIDs or other analgesic medication taken for any condition, will be included in the test group.
Willingness to sign the informed consent, follow the protocol and participate in clinical trial voluntarily.

Exclusion Criteria

Pregnancy and Lactation
Diabetes mellitus
Renal dysfunction
Liver diseases
Gastrointestinal diseases(Peptic ulcer disease)
Other types of arthritis
IHD and hypertension
History of surgery of the joint involved
Patients who will be unable to read/or understand the WOMAC questionnaire form

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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