Analgesic effect of topical gel Silymarin versus placebo in patients with knee osteoarthritis
Phase 3
- Conditions
- Condition 1: . Condition 2: Osteoarthritis of knee.Osteoarthritis of knee
- Registration Number
- IRCT20120215009014N498
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Age of 18 to 70 years
Mild to moderate knee osteoarthritis
Exclusion Criteria
Inflammation of the knee artery
Rheumatoid arthritis
History of knee surgery
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score. Timepoint: Before the intervention and 2 weeks later. Method of measurement: Using Visual Analog Scale (VAS).
- Secondary Outcome Measures
Name Time Method Probable side effects (reddish, pruritus). Timepoint: 2 weeks after the intervention. Method of measurement: By history taking and physical examination.