The effectiveness of oxycodone in knee replacement surgery
Phase 3
Recruiting
- Conditions
- Knee replacement surgery.
- Registration Number
- IRCT20220413054520N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients with knee osteoarthritis who have undergone primary knee replacement surgery
Exclusion Criteria
drug use
Antidepressants
anti-epilepsy
history of previous surgery on the affected knee
intraoperative fracture
reluctance of the patient to cooperate or continue follow-up
bmi above 40 and below From 20
alcohol consumption
taking any other analgesics other than prescribed
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient's knee pain. Timepoint: before intervention ,First day post op and 1 , 6 and 12 weeks after intervention. Method of measurement: Visual Analogue Scale score.;Knee function. Timepoint: before intervention and 8 and 12 weeks after intervention. Method of measurement: knee society score questionnaire.;Knee function. Timepoint: before intervention and 8 and 12 weeks after intervention. Method of measurement: Knee Injury and Osteoarthritis Outcome Score questionnaire.
- Secondary Outcome Measures
Name Time Method