A trial of blocking pain around knee joint by alcohol or phenol based intervention.
Phase 3
- Conditions
- Health Condition 1: M179- Osteoarthritis of knee, unspecified
- Registration Number
- CTRI/2024/07/070562
- Lead Sponsor
- il Ratan Sircar Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients from out patient department during the study primary osteoarthritis knee age between 40 to 60 years both gender clinically and radiologically confirmed for at least 3 months of duration
Exclusion Criteria
Patients with secondary osteoarthritis knee grade I and II osteoarthritis knee KL grading patients with uncontrolled comorbidities patients who got intraarticular injection in knee joint within last 3 months patients of syndrome complex not willing to give consent with psychiatric disorder of malignancy of bleeding diathesis with history of allergy of any of the pharmacological agents with infection either systemic or local history of knee surgery with anticoagulant medications
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method General Objective is to evaluate reduction of pain in VAS Scale in grade III and grade IV osteoarthritis Knee as per KL grading <br/ ><br>Specific Objectives are to assess the improvement in knee pain and quality of life in KOOS Scale to find out the improvement in the sleep quality in Pittsburgh sleep quality index PSQI scale to identify the side effects if any due to intervention <br/ ><br>Timepoint: outcome will be assessed at baseline or 0 week 4th week 12th week and at 24th week
- Secondary Outcome Measures
Name Time Method To assess the improvement in knee pain quality of life in KOOS Scale to find out the improvement in sleep quality in Pittsburgh sleep quality index PSQI scale to identify the side effects if any due to interventionTimepoint: Outcome will be assessed at baseline or 0 week 4th week 12th week 24th week