Comparing pain relief during & after laparoscopic surgeries by using multiple approaches to pain management using narcotic free medications
Phase 4
Not yet recruiting
- Conditions
- Health Condition 1: K352- Acute appendicitis with generalized peritonitisHealth Condition 2: K800- Calculus of gallbladder with acutecholecystitisHealth Condition 3: N938- Other specified abnormal uterine and vaginal bleedingHealth Condition 4: K469- Unspecified abdominal hernia without obstruction or gangrene
- Registration Number
- CTRI/2023/06/053482
- Lead Sponsor
- Rajarajeswari Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA I and II patients of either sex.
2. Patients aged between 18 to 70 years
3. Patients undergoing elective laparoscopic abdominal surgeries.
Exclusion Criteria
1. Patientâ??s refusal.
2. Pregnant and lactating women, patients with epilepsy and mentally unstable patients.
3. ASA 3 and ASA 4 patients.
4. Allergy to study drugs
5. Patient on opioids, sedatives, beta-blockers
6. Coagulopathy
7. Infection at the site of block
8. Neuroâ??psychiatric disorders
9. Hepatic and renal dysfunction
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare opiod free anaesthesia technique with opioid based anaesthesia on peri-operative pain relief.Timepoint: Intraoperative pain will be assessed using hemodynamic parameters from the time of induction till end of surgery. <br/ ><br>Postoperative pain will be assessed using 0 to 10 visual analogue score at 5, 15, 30, 60 mins, 2, 4, 6, 8, 10, 12, 16, 20, 24 hrs.
- Secondary Outcome Measures
Name Time Method Suppression of hemodynamic responses during surgery. <br/ ><br>Perioperative opioid consumption. <br/ ><br>Duration of analgesia & time for first rescue analgesic request. <br/ ><br>Postoperative nausea & vomiting. <br/ ><br>Sleep quality. <br/ ><br>Patient satisfaction. <br/ ><br>Adverse effects if any.Timepoint: Total opioid consumption intraoperatively will be recorded. Duration till first rescue analgesic request & total analgesic consumption in 24 hours will be noted. Postoperative nausea, vomiting, sleep quality and adverse events during first 24 hours will be recorded. Patient satisfaction will be assessed according to comfort VAS scale.