Image guided pain relief with local anaesthesia in patients undergoing laparoscopic abdominal surgeries
Phase 4
Completed
- Conditions
- Health Condition 1: - Health Condition 2: R198- Other specified symptoms and signsinvolving the digestive system and abdomen
- Registration Number
- CTRI/2020/10/028498
- Lead Sponsor
- Himalayan Institute Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
1.American society of anaesthiology ( ASA ) physical status 1 and 2
2.patients undergoing elective laparoscopic abdominal surgeries.
3, weight > 50kgs
Exclusion Criteria
1.ASA physical status 3 and 4 and emergency surgeries.
2. Patients refusal for regional anesthesia.
3.laparoscopic surgeries converted to open surgery
4. pregnant and lactating mothers
5.Allergy and contraindication to study drugs.
6.Hepatic , renal and cardiopulmonary abnormalities.
7. Bleeding diathesis
8.Local site infections
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 quadratus lumborum and block and erector spinae block following laparoscopic abdominal surgeries.Timepoint: 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 24hrs interval respectively
- Secondary Outcome Measures
Name Time Method To study hemodynamic and adverse effects after ultrasound guided erector spinae block and quadratus lumborum block in patients undergoing laparoscopic abdominal surgries.Timepoint: preoperatively ( baseline), immediately after block 0,5,10,15,20,25,30, during induction and intubation , intraoperatively at 5,10,15,20,25,30,45,60,75,90,105,120mins and postoperatively at 0,15,30mins, 1,2,3,4,6,8,10,12,16,20 and 24 hrs interval respectively.