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Sambucus ebulus effect on knee Osteoarthritis

Phase 3
Conditions
knee osteoartritis.
Primary arthrosis of other joints
Registration Number
IRCT2014080318494N1
Lead Sponsor
Vice Chancellor for research, Shahid Sadoughei University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
94
Inclusion Criteria

Inclusion Criteria: age: 30-60 years; A history of knee pain for at least 3 months; Mild to moderate Osteoarthritis (grade 1 and 2) based on Kellegren-Lawrence grading scale;

Exclusion Criteria

1-Allergy to Sambucus ebulus & Diclofenac gel; Skin lesions in the knee; Osteoarthritis secondary to Rheumatic disease such as Rheumatoid Arthritis, Gout, Infectious Arthritis, Metabolic Arthritis, Traumatic Arthritis; Knee joint replacement surgery; Oral and topical steroid therapy within 14 days prior to study; Intra-articular steroid injections within 90 days prior to study; Pregnancy and Lactation; Addiction to alcohol and drugs; Radiculopathy and Neuropathy

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Baseline, 2 and 4 weeks after intervention. Method of measurement: WOMAC questionnaire.;Stiffness. Timepoint: Baseline, 2 and 4 weeks after intervention. Method of measurement: WOMAC questionnaire.
Secondary Outcome Measures
NameTimeMethod
Physical function. Timepoint: Baseline, 2 and 4 weeks after intervention. Method of measurement: WOMAC questionnaire.
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