A study to compare pain relieving effect of intrathecal morphine and adductor canal block in patients undergoing knee ligament repair surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: M236- Other spontaneous disruption of ligament(s) of knee
- Registration Number
- CTRI/2024/08/071945
- Lead Sponsor
- Aiims Kalyani
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients of Age 18-65 years of both sexes with American Society of Anesthesiologist (ASA) 1 and 2 undergoing knee arthroplasty under spinal anesthesia
Exclusion Criteria
total surgical duration more than 3 hours
ASA 3 and 4
refuse to consent for spinal anesthesia
history of coagulopathy with raised INR more than or equal to 1.5
local infection at needle insertion site
history of psychiatric illness and on antipsychotic medications
history of opioid dependence
history of chronic pain
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cumulative morphine equivalent consumption <br/ ><br>Timepoint: 24 hours <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.Numeric Rating scale for pain <br/ ><br>2. Time to first postop mobilisation <br/ ><br>3. Quadriceps muscle strength <br/ ><br>4. Adverse effects (Nausea, Vomitting, pruritus) <br/ ><br> <br/ ><br>Timepoint: 1.Numeric Rating scale for pain at 0,2,4,6,8,12 & 24 hours <br/ ><br>2. Time to first postop mobilisation <br/ ><br>3. Quadriceps muscle strength at 6,8,12 & 24 hours <br/ ><br>4. Adverse effects (Nausea, Vomitting, pruritus) <br/ ><br> <br/ ><br>