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To study effect of adductor canal infiltration given by operating surgeon on pain management and recovery in patients undergoing total knee replacement.

Not Applicable
Completed
Conditions
Health Condition 1: M171- Unilateral primary osteoarthritisof knee
Registration Number
CTRI/2020/03/024180
Lead Sponsor
Dr Rajesh Maniar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
120
Inclusion Criteria

i)Unilateral total knee replacement

ii)Primary total knee replacement

iii)Spinal anesthesia only

iv)Willing to participate in study and sign consent form

Exclusion Criteria

i)Bilateral Total Knee Replacement

ii)Revision Total Knee Replacement

iii)Medical conditions (eg : chronic kidney disease) requiring alteration in pain management protocol

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1)Pain by Visual Analogue scale <br/ ><br>2) Analgesic consumption (PCA consumption)Timepoint: 1) Preoperatively, <br/ ><br>6 hours Postoperatively <br/ ><br>Postoperative Day 1, <br/ ><br>Postoperative Day 2, <br/ ><br>Postoperative Day 3 <br/ ><br>2) 6 Hours postoperatively <br/ ><br>Postoperative Day 1, <br/ ><br>Postoperative Day 2, <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1) Flexion <br/ ><br>2) TUG test <br/ ><br>3) Time to meet discharge in hoursTimepoint: 1) Preoperatively, <br/ ><br>Post operative Day 1, <br/ ><br>Post operative Day 2, <br/ ><br>Postoperative Day 3, <br/ ><br>Post operative Day 14 <br/ ><br>2) Preoperatively, <br/ ><br>Post operative Day 1, <br/ ><br>Post operative Day 2, <br/ ><br>Postoperative Day 3, <br/ ><br>Post operative Day 14 <br/ ><br>
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