Ayurvedic treatment for pai
Not Applicable
- Conditions
- Health Condition 1: null- ï?µEighty (80) patients with MSD, meeting all inclusion/exclusion criteria will be included in the study
- Registration Number
- CTRI/2017/09/009907
- Lead Sponsor
- MB Life Scienes Pvt Ltd New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with musculoskeletal pain and swelling, fulfilling the diagnostic criteria of MS, willing to give consent for participating in the study. Patients who are currently on analgesics/NSAID, will be given a washout period of 7days prior to recruitment
Exclusion Criteria
Patients having severe MSD, those who are suffering from dermatitis or had a history of dermatitis, pregnant and lactating women, any other conditions which in the opinion of investigator will places the subject at risk or will influence the conduct of study or interpretation of results
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Before and after the treatment period of 7 days <br/ ><br>Changes in following parameters between day 1 and day 7: <br/ ><br>â?¢Subjective parameters: Pain (VAS), Tenderness, Shotha (swelling/Inflammation), Stabdata (Stiffness), Physician Global Assessment <br/ ><br>â?¢Objective parameters: Range of Motion (Goniometer) <br/ ><br> At screening: RA, CRP, Serum Uric acid <br/ ><br> Safety Parameters: CBC, LFT, RFT (base line and 7th day) (Only 50% of Patients) <br/ ><br>Timepoint: Day 0, 8, 22,37
- Secondary Outcome Measures
Name Time Method Assessment of subsidence after treatment period during the follow-up period up to 30 days. <br/ ><br>Subjective parameters will be assessed on day 15th and 30th day <br/ ><br>Timepoint: Day0, 8, 22 and 37