Effect of saqez cream on knee osteoarthritis
- Conditions
- Osteoarthritis.Primary arthrosis of other joints
- Registration Number
- IRCT201506073106N26
- Lead Sponsor
- Islamic Azad University, Pharmaceutical Sciences Branch
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 85
Patient's written consent; radiographic changes; primary knee osteoarthritis grade 2 and 3; age between 35 – 85; patients who did not receive topical treatment or received previous topical treatment for at least two weeks before they start on this trial. All patients must be stable on their current oral therapy.
Exclusion criteria:
Patients who needs more than 2 grams of acetaminophen in order to control pain; Those who need to use other oral or intravenous analgesics; Unwilling to continue or to participate in the study any further; Sensitivity to study drugs; Patients with other bone joint disorders: ( Rhumatoid Arthrities, Gout, Pseudo Gout, Infected Arthrities, Metabolic Arthrities, Traumatic Arthrities ) ; Infections and malignancy disease; Joint replacement; Fibro myalgia; Knee corticosteroid injection in the past 3 months, Pregnancy, oral and local use of corticosteroids; Pationts with active Renal, Liver and Peptic Ulcer Disease; Alcohol addicted; Drug Abuse
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Physical function. Timepoint: 2 Weeks,6 weeks and 12 weeks after baseline. Method of measurement: Womac questionaries.;Stiffness. Timepoint: 2 Weeks,6 weeks and 12 weeks after baseline. Method of measurement: Womac questionaries.;Pain. Timepoint: 2 Weeks,6 weeks and 12 weeks after baseline. Method of measurement: Womac questionaries.
- Secondary Outcome Measures
Name Time Method