Pain relief for single knee replacement surgery
Not Applicable
- Conditions
- Health Condition 1: null- Patients scheduled for unilateral total knee arthroplasty
- Registration Number
- CTRI/2017/05/008481
- Lead Sponsor
- Army Hospital Research and Referral Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
ASA I-III
BMI 20-30 kg/m2
Patients scheduled for elective unilateral total knee arthroplasty
Exclusion Criteria
Contraindication to subarachnoid block or allergy to any of the study drugs;
Known coagulopathy, local infection at block site;
Patients in whom the nerve block could not be performed at per the procedure described in the methodology;
Renal dysfunction
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of post-operative analgesiaTimepoint: 24 hr
- Secondary Outcome Measures
Name Time Method Any adverse effects , if anyTimepoint: 24 hr;Level of patient satisfactionTimepoint: At 24 hr;Success of early ambulation in terms of steps walked by the patient after surgeryTimepoint: 24 hr;Total 24 hr opioid consumption in the form of intravenous tramadolTimepoint: 24 hr