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

NCT ID: NCT05632991

Last Updated: 2024-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-01

Study Completion Date

2024-01-01

Brief Summary

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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

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Conditions

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Analgesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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External oblique intercostal plane block

Ultrasound-guided External oblique intercostal plane block before surgery

Group Type ACTIVE_COMPARATOR

ultrasound guided external oblique intercostal plane block

Intervention Type OTHER

ultrasound guided external oblique intercostal plane block 20 ml local anesthetic each side

Subcostal Transversus Abdominis Plan Block Group

Ultrasound-guided Subcostal Transversus Abdominis Plan Block Group

Group Type ACTIVE_COMPARATOR

Subcostal Transversus Abdominis Plan Block Group

Intervention Type OTHER

ultrasound guided Subcostal Transversus Abdominis Plan Block Group 20 ml local anesthetic each side

Interventions

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ultrasound guided external oblique intercostal plane block

ultrasound guided external oblique intercostal plane block 20 ml local anesthetic each side

Intervention Type OTHER

Subcostal Transversus Abdominis Plan Block Group

ultrasound guided Subcostal Transversus Abdominis Plan Block Group 20 ml local anesthetic each side

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ataturk University

OTHER

Sponsor Role lead

Responsible Party

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Ali Ahiskalioglu

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Atatürk University

Erzurum, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Woldu SL, Weinberg AC, Bergman A, Shapiro EY, Korets R, Motamedinia P, Badani KK. Pain and analgesic use after robot-assisted radical prostatectomy. J Endourol. 2014 May;28(5):544-8. doi: 10.1089/end.2013.0783. Epub 2014 Jan 30.

Reference Type BACKGROUND
PMID: 24400824 (View on PubMed)

Leitao MM Jr, Malhotra V, Briscoe G, Suidan R, Dholakiya P, Santos K, Jewell EL, Brown CL, Sonoda Y, Abu-Rustum NR, Barakat RR, Gardner GJ. Postoperative pain medication requirements in patients undergoing computer-assisted ("Robotic") and standard laparoscopic procedures for newly diagnosed endometrial cancer. Ann Surg Oncol. 2013 Oct;20(11):3561-7. doi: 10.1245/s10434-013-3064-9.

Reference Type BACKGROUND
PMID: 23797751 (View on PubMed)

Other Identifiers

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ataunilapcholecystectomy

Identifier Type: -

Identifier Source: org_study_id

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