To observe pain sparing effect of thigh nerve block in patients undergoing knee surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/04/018412
- Lead Sponsor
- Department of Anaesthesia and Intensive care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age between 18 to 60 years
2. American Society of Anesthesiologist (ASA) physical status I and II of either sex.
3. BMI >= 20 to <= 30 kg m-2 4. Patients scheduled for ACL reconstruction surgery.
Exclusion Criteria
1. Patientâ??s inability to understand VAS.
2. Patients with coagulopathy and bleeding disorders.
3. Pre-existing peripheral neuropathy.
4. Patientshaving history of substance abuse.
5. Pre-existing local infection at the site of block.
6. Pregnant and lactating women.
7. Contraindication to study drugs: Diclofenac, Ropivacaine.
8. Patients having hemodynamic instability, hypotension, bradycardia, hepatic dysfunction.
9. Patients on regular chronic pain management drugs for the last three months.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the time to first rescue analgesia in patients receiving adductor canal block following anterior cruciate ligament surgeryTimepoint: Post operative block placement patient will be monitored at 0,5,10,15,20,30,60 minutes followed by 2,4,6,8,12 and at 24-hour interval
- Secondary Outcome Measures
Name Time Method Patients will be monitored for Blood Pressure, Pulse Rate, Respiratory Rate, VAS4 at rest pain, VAS on movement (pain on flexion of knee at 45-600), first rescue analgesic requirement, total analgesic consumption, nausea, vomiting or any other complaintTimepoint: Post operative block placement patients will be monitored for BP, PR, RR, VAS4 at rest pain, VAS on movement (pain on flexion of knee at 45-60), 1.first rescue analgesic requirement, 2.total analgesic consumption, <br/ ><br>3.nausea, vomiting or 4.any other complaint immediately after block in 0,5,10,15,20,30,60 minutes followed by 2,4,6,8,12 and at 24-hour interval