Comparison of effectiveness of postoperative pain relief in general anaesthesia between opioid group and without opioid using nerve block, continuous intravenous lidocaine and magnesium injection.
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/10/046738
- Lead Sponsor
- AARUPADAI VEEDU MEDICAL COLLEGE AND HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
1. ASA I and ASA II Patients
2. Age between 18 years to 60 years
3. Patient scheduled for elective laparoscopic abdominal surgeries - appendicectomy and cholecystectomy.
Exclusion Criteria
1. Patient not willing to participate in the study.
2. ASA III and above.
3. Patients with coagulation abnormality.
4. Patients with hepatic, cardiac, liver and renal illnesses.
5. BMI > 35kg/m2.
6. Pregnant women.
7. Hypersensitivity to any of the drugs used (Lidocaine, bupivacaine, propofol).
8. Surgeries lasting more than 2 hours.
9. Emergency surgeries.
10. Infection at the site of fascial plane block.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Increased post operative analgesia duration in Opioid free groupTimepoint: 12 - 24 hours postoperative period
- Secondary Outcome Measures
Name Time Method Haemodynamic stability <br/ ><br>Less postoperative sedation <br/ ><br>Less incidence of nausea, vomiting, pruritusTimepoint: Intraoperative perioperative, 0-24 hours postoperative period