Study to compare external oblique intercostal fascial plane block and erector spinae plane block in patients undergoing open abdominal surgeries by assessing pain after surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063615
- Lead Sponsor
- Aiims Patna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients 18 -75 years,
American Society of Anesthesiologists-physical status (ASA-PS) I–II undergoing open
upper abdominal surgery with Unilateral Subcostal incision
Patients willing to give written informed consent
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess and compare 24-hour postoperative opioid consumption in ESP block group and <br/ ><br>EOI block group via numerical rating scale (NRS)Timepoint: To assess and compare 24-hour postoperative opioid consumption in ESP block group and <br/ ><br>EOI block group via numerical rating scale (NRS) at 30 minutes, 2 hours, 4 hours, 8 hours, 12 hours, 16 hours and 24 hours.
- Secondary Outcome Measures
Name Time Method Time to first rescue analgesia. <br/ ><br>Numerical rating scores of pain (rest and cough) in first 24-hour postoperative period <br/ ><br>Total intraoperative opioid consumption <br/ ><br>Postoperative opioid consumption <br/ ><br>Timepoint: From the time of administration of block to first need of use of analgesic administration <br/ ><br>30 mins, 2,4,8,12,16,24 hours. <br/ ><br>from the time of administration of block to end of surgery <br/ ><br>at 4, 8, 12, 16 hours <br/ ><br>