Management of Knee Osteoarthritis with Wet-Cupping
Phase 2
- Conditions
- Health Condition 1: null- Knee Osteoarthritis
- Registration Number
- CTRI/2017/07/009046
- Lead Sponsor
- Jamia Hamdard
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients of knee osteoarthritis with Subjective pain intensity of 20 at baseline on visual analogue scale(VAS)
Exclusion Criteria
Age below 35 and above 70 yrs
Patients with DM, hepatic, renal or cvs disorders
Patient on anticoagulant therapy or Haemophiliacs or with severe Anaemia
Pregnant and lactating mothers
ESR > 40mm/hr
Terminally ill patients with infectious diseases like AIDS and Tuberculosis etc
Patients who fail to give written consent
Patients with stage 3 and stage 4 of knee osteoarthritis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS <br/ ><br>Knee Injury Osteoarthritis Outcome Score(KOOS) <br/ ><br>Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Index <br/ ><br>Active range of motion using GoniometerTimepoint: 0 Day,7th Day, 14th Day,21st Day, 28th Day
- Secondary Outcome Measures
Name Time Method rinarypyridinoline(picomole/µm creatinine) <br/ ><br>X ray Knee joint AP & Lateral (Kellgren-Lawrence grading Scale) <br/ ><br>Safety parameters include-CBC with ESR,LFT,KFT,Blood sugar fasting and PP,BT & CT,Urine R/MTimepoint: 0 Day,28th Day