A clinical trial to study the effect of two dosage forms of a herb(Leonotis nepetifolia)in patients with Osteoarthritis
Phase 1
- Conditions
- Health Condition 1: null- Osteoarthritis
- Registration Number
- CTRI/2013/03/003465
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Patients with symptoms of sandhivata
Exclusion Criteria
Other types of sandhi vyadhis like ama vata, vata rakta and koshtrukasirsha
Uncontrolled systemic diseases like Hypertension, diabetes mellitus and kidney disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Baseline evaluation will be done based on the symptoms of Sandhivata- sandhi shula, sandhi shotha,akunchana prasarana vedana, sandhigraha, sandhisputana, sparshasahatva. Scoring pattern will be 0-no symptom, 1-mild symptom,2 moderate symptom,3-severe The evaluation will be repeated at week 3 and week 6(end point)Timepoint: Baseline <br/ ><br>Week 3 <br/ ><br>End point at week 6
- Secondary Outcome Measures
Name Time Method Visual Analog scale for Pain and WOMAC Qestionnaire will be done at Baseline and End pointTimepoint: Baseline and End point