External Oblique Intercostal Plane Block vs. Transversus Abdominis Plane Block for Laparoscopic Cholecystectomy

Not Applicable

Completed

• Conditions: Analgesia
• Interventions: Other: ultrasound guided external oblique intercostal plane block; Other: Subcostal Transversus Abdominis Plan Block Group

• Registration Number: NCT05632991
• Lead Sponsor: Ataturk University

Brief Summary

The laparoscopic approach has become the gold standard for many abdominal surgical procedures, including cholecystectomy. Compared to laparotomy, laparoscopy allows smaller incisions, reduces perioperative stress response, reduces postoperative pain, and results in shorter recovery time.

However, anaesthesia concerns in patients undergoing laparoscopic surgery are different from patients undergoing open abdominal surgery.

The aim of this study is to investigate the effect of the external oblique intercostal block, which is a new block, on postoperative pain score and opioid consumption.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-11-21
• Study First Submitted QC: 2022-11-21
• Study Start: 2022-12-01
• Study First Posted: 2022-12-01
• Primary Completion: 2023-09-01
• Study Completion: 2024-01-01
• Status Verified: 2024-03
• Last Update Submitted: 2024-03-29
• Last Update Posted: 2024-04-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

• American Society of Anesthesiologist's physiologic state I-III patients
• Laparoscopic cholecystectomy

Exclusion Criteria

• Chronic pain bleeding disorders renal or hepatic insufficiency patients on chronic non-steroidal anti-inflammatory medications emergency cases

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
External oblique intercostal plane block	ultrasound guided external oblique intercostal plane block	Ultrasound-guided External oblique intercostal plane block before surgery
Subcostal Transversus Abdominis Plan Block Group	Subcostal Transversus Abdominis Plan Block Group	Ultrasound-guided Subcostal Transversus Abdominis Plan Block Group

Primary Outcome Measures

Name	Time	Method
Postoperative opioid consumption	first 24 hours	First 24 hours total fentanyl consumption with patient controlled analgesia

Secondary Outcome Measures

Name	Time	Method
Visual analog pain score	postextubation 0-24 hours	Post operative pain will be evaluated with a Visual Analogue Scale (VAS) score of 0-10 (0= no pain and 10= worst imaginable pain)

Trial Locations

Locations (1)

Atatürk University; 🇹🇷 Erzurum, Turkey