Image guided pain relief with local anaesthesia in patient undergoing laparoscopic cholecystectomy
Phase 4
Completed
- Conditions
- Health Condition 1: K800- Calculus of gallbladder with acutecholecystitis
- Registration Number
- CTRI/2020/07/026312
- Lead Sponsor
- Himalayan Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 105
Inclusion Criteria
1. ASA physical status I and II of either sex
2. Age between 18-65 years
3. Scheduled for laproscopic cholecystectomy surgery
Exclusion Criteria
1. American Society of Anesthesiologist (ASA) physical status III and IV and Emergency surgeries
2. Patient refusal for regional anesthesia.
3. Presence of spine deformities.
4. Allergy or contraindication to study drugs.
5. Pregnancy, lactating mothers.
6. BMI more than or equal to 35 kg/m2.
7. Chronic pain
8. Hepatic, renal or cardiopulmonary abnormality, uncontrolled diabetes, seizures
9. Bleeding diathesis
10.Local skin site infection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study post operative pain and fentanyl sparing effect after erector spinae block following laparoscopic cholecystectomyTimepoint: To study total fentanyl consumption over 24 hrs and to study pain intensity at 0,15,30 mins, 1,2,3,4,6,8,10,12,16,20 and 24 hrs interval respectively
- Secondary Outcome Measures
Name Time Method To study hemodynamics and adverse effects after ultrasound guided erector spinae block in patients undergoing laparoscopic cholecystectomy.Timepoint: Preoperatively (baseline), immediately after block 0.5,10,15,20,25,30, during induction and intubation, intraoperatively at 5,10,15,20,25,30,45,60,75,90,105,120 mins and postoperatively at 0,15,30 mins, 1,2,3,4,6,8,10,12,16,20 and 24 hrs interval respectively.