CTRI/2025/01/079146
Completed
Phase 4
External oblique intercostal plane block versus Erector spinae plane block for post operative analgesia in open hepatopancreatic biliary surgeries- a randomized control trial
Institute of liver and biliary sciences1 site in 1 country60 target enrollmentStarted: February 5, 2025Last updated:
Overview
- Phase
- Phase 4
- Status
- Completed
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- To compare the postoperative fentanyl
Overview
Brief Summary
Hypothesis; external oblique intercostal plane block is as effective as erector spinae plane block in providing analgesia in patients undergoing open hepatopancreatic biliary surgeries
Study population - 60 patients undergoing open hepatopancreatic biliary surgeries
Group A- 30 patients- USG guided External oblique intercostal plane block.
Group B- 30 patients- USG guided Erector spinae plane block.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Age 18-60 years , undergoing open hepatopancreatic and biliary surgery, who give consent.
Exclusion Criteria
- •Patient refusal Infection at site of administration Allergy to local anaesthetics Insufficient comprehension of the use of Patient controlled Analgesia ( PCA) machine Coagulopathy and thrombocytopenia (Platelet count less than 80,000/ microL ).
Outcomes
Primary Outcomes
To compare the postoperative fentanyl
Time Frame: upto 24 hours in the post operative period
consumption at 24 hours between the external oblique intercostal plane block and Erector spinae plane block groups
Time Frame: upto 24 hours in the post operative period
Secondary Outcomes
- To compare the intraoperative IV fentanyl requirements in both the groups.(To compare the postoperative pain using NRS in both the groups)
Investigators
Dr Kiran Premraj
Institute of Liver and Biliary sciences
Study Sites (1)
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