comparison of Pain relief after total knee replacement surgery between adductor canal block and local intraarticular infiltratio
Not Applicable
Completed
- Conditions
- Health Condition 1: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2018/10/016113
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 64
Inclusion Criteria
ASA physical status I-III scheduled for elective primary unilateral knee arthroplasty
Exclusion Criteria
1.Age > 80 years
2.ASA IV / V
3.Bilateral / Revision TKA
4.Morbid obesity (BMI >= 40 )
5.History of focal neurological deficit
6.History of sensory or motor disorders of limb to be operated
7.History of allergy to local anaesthetics , clonidine
8.History of regular opioid use
9.Local site infection
10.Patient refusal to partake in the study.
11.Contraindication to spinal anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To estimate the total morphine consumption in the three groupsTimepoint: 24 hours postopertively
- Secondary Outcome Measures
Name Time Method To assess pain scores at rest and movement using visual analogue scaleTimepoint: 0,4,8,12,24 hours postoperatively;To assess patient satisfactionTimepoint: 24 hours postoperatively;To compare the side effects associated with morphine consumption in the three groupsTimepoint: 24 hours postoperatively;To estimate the time to first use of patient controlled analgesia deviceTimepoint: 24 hours postoperatively;To estimate the worst pain during and time taken to perform the timed get up and go (TUG) testTimepoint: 24 hours postoperatively