Skip to main content
Clinical Trials/CTRI/2025/02/080148
CTRI/2025/02/080148Not yet recruitingPhase 2

External oblique intercostal block vs Oblique subcostal transversus abdominis plane block for postoperative pain management in surgeries with modified Makuuchi incision- A Randomised Controlled Study (OBLIQUES

Angshuman Rudrapal1 site in 1 country70 target enrollmentStarted: February 15, 2025Last updated:

Trial Snapshot

Phase
Phase 2
Status
Not yet recruiting
Sponsor
Enrollment
70
Locations
1
Primary Endpoint
24 hours intravenous morphine consumption in mg

Study Overview

Brief Summary

The modified Makuuchi incision involves a vertical midline cut that meets a horizontal incision at the umbilical level involving T6-T10 dermatomes. The horizontal incision takes a reversed L-shape, following the contour of the abdominal skinfold, ending at the midpoint between the lowest rib and the anterior superior iliac spine. This incision is often employed for upper abdominal surgeries like radical cholecystectomy, hepatectomy, Whipple’s procedure and radical nephrectomy. The institutional practice is to give bilateral oblique subcostal TAP block in these surgeries for postoperative analgesia as a part of an enhanced recovery protocol. This blocks the anterior cutaneous branches but spares the lateral cutaneous branches of T6-T10 intercostal nerves and hence does not cover the

horizontal part of the incision. The external oblique intercostal block (EOIB),initially described by Elsharkawy et al, is a novel fascial plane block indicated for upper abdominal

procedures. It blocks the anterior and lateral cutaneous branches of the T6–T10 intercostal nerves and can be performed easily under ultrasound guidance due to the superficial location of the fascial plane between the external oblique and intercostal muscles. To our knowledge, analgesic efficacy of EOIB vs OSTAP in surgeries involving modified Makuuchi

incision has not been investigated yet in a randomised controlled trial. So, this single centre, randomised, double-blind controlled trial has been designed to investigate the analgesic

efficacy of EOIB vs OSTAP in surgeries involving modified Makuuchi incision. 35 patients will be analysed in each group. Eligible patients undergoing elective abdominal surgeries with modified Makuuchi incision or reversed L- shaped incision will be included in our study. Our primary outcome is the 24 hour postoperative morphine consumption, while secondary outcomes include 48-hours and 72-hours intravenous morphine consumption in mg, QOR-15 score at postoperative day 1 and postoperative day 3, Postoperative rescue fentanyl requirements in mcg in the first 48 hours, Numeric Rating Scale (NRS) of static and dynamic pain, Modified Ramsay Sedation Score at various time intervals, complications like postoperative respiratory depression, PONV, pruritus, time to enteric resumption, ambulation and flatus pass, patient satisfaction score, length of hospital stay.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 80.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients undergoing elective abdominal surgeries with modified Makuuchi incision or reversed L- shaped incision.
  • American Society of Anaesthesiology Physical Score (ASA-PS) score of I.

Exclusion Criteria

  • Patients requiring postoperative mechanical ventilation.
  • Contraindications to spinal anaesthesia Contraindications to study medication Documented obstructive sleep apnea Patients with life threatening arrhythmias Patients with left ventricular ejection fraction less than 40% Coagulopathy Pre Existing neurological illness Significant liver dysfunction (liver enzymes more than 3 times normal) Significant renal dysfunction (creatinine more than 2 times normal) Psychiatric illness Opioid abuse Patients receiving systemic opioids for chronic pain within last 30 days.

Outcomes

Primary Outcomes

24 hours intravenous morphine consumption in mg

Time Frame: 24 hours intravenous morphine consumption in mg

Secondary Outcomes

  • 1. 48-hours and 72-hours intravenous morphine consumption in mg(2. QOR-15 score at postoperative day 1 and postoperative day 3)

Investigators

Sponsor
Angshuman Rudrapal
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Angshuman Rudrapal

Tata Medical Center

Study Sites (1)

Loading locations...

Similar Trials