The effect of L carnitine in women with knee osteoarthritis
Phase 2
- Conditions
- knee osteo arthritis.Primary generalized (osteo)arthrosis
- Registration Number
- IRCT2017011932026N2
- Lead Sponsor
- Vice Chancellor for research of School of Public Health, Shahid Sadoughi University of Medical Scien
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 76
Inclusion Criteria
women? age between 45 to 70? Early detection of osteoarthritis? body mass index more than25? Lack of weight loss diets over the past three months? lack of participate in the intervention program the past three months
Exclusion: heart disease? hypothyroidism? rheumatoid arthritis? hepatic disease?kidney disease and knee sergury
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: before intervention and 12 weeks after the intervention. Method of measurement: womac questionnaire.;Lipid profile(HDL, LDL, TG, Cho). Timepoint: before intervention and 12 weeks after the intervention. Method of measurement: with special kits.;CRP. Timepoint: before intervention and 12 weeks after the intervention. Method of measurement: with special kits.;Malondialdehyde. Timepoint: before intervention and 12 weeks after the intervention. Method of measurement: with special kits.
- Secondary Outcome Measures
Name Time Method Waist, Hip circumference. Timepoint: before intervention and 12 weeks after the intervention. Method of measurement: meter.;Weight, fat mass, free fat mass. Timepoint: before intervention and 12 weeks after the intervention. Method of measurement: Omron digital Scale(BF11).