A Clinical trial to study the safety and efficacy of â??Pachaikarpoora Vadagamâ?? (internal) and â??Vaeppa Ennaiâ?? (External) in the treatment of Osteoarthritis-knee joint.
Phase 2
Completed
- Conditions
- Health Condition 1: M170- Bilateral primary osteoarthritis of knee
- Registration Number
- CTRI/2018/06/014441
- Lead Sponsor
- ATIONAL INSTITUTE OF SIDDHA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
•Patients having symptoms of arthritis of both knee joints, Pain, swelling, stiffness, crepitations, restricted movements of both knee joints.
•Patients who are willing to undergo radiological investigation, Laboratory investigations.
•Patients willing to sign the informed consent stating that he/she will conscientiously stick to the treatment during 48days but can opt out of the trial of his/her own conscious discretion.
•Willing to co operate to take photographs whenever required with his/her consent.
Exclusion Criteria
•Cardiac diseases
•Diabetes Mellitus
•Hypertension
•Rheumatoid arthritis
•Use of Narcotics
•Pregnancy and lactation
•History of trauma
•Patient with any other serious systemic illness
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PAIN REDUCTION DETERMINED BY UNIVERSAL PAIN ASSESSMENT SCALE. <br/ ><br>RESTRICTED MOVEMENT ASSESSMENT SCALE. <br/ ><br>Timepoint: 48 DAYS <br/ ><br>
- Secondary Outcome Measures
Name Time Method REDUCTION OF CLINICAL SYMPTOMSTimepoint: 48 DAYS