External Oblique Intercostal Plane Block Versus Subcostal Transversus Abdominis Plane Block in Supra-umbilical Surgical Incisions

Not Applicable

Completed

• Conditions: Pain, Postoperative

• Registration Number: NCT05432557
• Lead Sponsor: Benha University

Brief Summary

Various newer techniques have been proposed to enhance analgesia in upper abdominal region. The subcostal transverse abdominis plane (SCTAP) block is the deposition of local anesthetic in the transverse abdominis plane inferior and parallel to the costal margin. There is a growing consensus that the SCTAP block provides better analgesia for upper abdominal incisions than the traditional transverse abdominis plane block.

The External oblique intercostal plane (EOIP) block is a novel technique reported by Hamilton et al. performed EOPB by administering LA superior or deep of the external oblique muscle from the sixth intercostal space leading to the blockage of thoracoabdominal nerves at T6-T10. It has several attractive aspects such as easy sono-anatomy ribs one strip of muscle so easy to demonstrate even in obese patients, there is a bony backstop, easy expandable fascial plane that can accommodate a catheter and it is shallow block with no big vessels nearby.

Detailed Description

Not available

Study Timeline

• Study Start: 2022-06-20
• Study First Submitted: 2022-06-21
• Study First Submitted QC: 2022-06-24
• Study First Posted: 2022-06-27
• Primary Completion: 2022-12-10
• Study Completion: 2023-04-20
• Status Verified: 2024-12
• Last Update Submitted: 2024-12-16
• Last Update Posted: 2024-12-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

1. American Society of Anesthesiologists (ASA) physical status grade I -II,
2. Scheduled to undergo elective supra-umbilical surgeries under GA (epigastric herniotomy- gastrectomy- open cholecystectomy- nephrectomy).

Exclusion Criteria

1. Allergy to local anesthetics,
2. Infection at the site of injection,
3. Coagulopathy,
4. Chronic pain syndromes,
5. Prolonged opioid medication,
6. Patients who received any analgesic 24 h before surgery.
7. Chronic liver disease, chronic renal disease, and cognitive impairment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
amount of postoperative morphine consumed	24 hours postoperatively
First postoperative analgesics request	24 hours postoperatively

Secondary Outcome Measures

Name	Time	Method
Postoperative pain score	at 1, 2,4 , 8, 16 and 24 hours postoperatively	pain evaluated by VAS (visual analogue score).
incidence of complications related to the block	24 hours postoperatively	agitation, dizziness, tinnitus, tremors, and numbness.
Incidence of Postoperative nausea & vomiting (PONV)	24 hours postoperatively	Number of patients developing PONV

Trial Locations

Locations (1)

Samar Rafik Amin; 🇪🇬 Banhā, Qalubia, Egypt