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Clinical Trials/NCT05614921
NCT05614921
Completed
Not Applicable

Ultrasound Guided External Oblique Intercostal Plane Block vs. Wound Infiltration for Laparoscopic Sleeve Gastrectomy: Prospective Randomized Study

Ataturk University1 site in 1 country60 target enrollmentNovember 15, 2022
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Ataturk University
Enrollment
60
Locations
1
Primary Endpoint
Postoperative opioid consumption
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The morbidity and mortality associated with being overweight or obese have been known to the medical profession since Hippocrates, more than 2500 years ago.

Pain that develops following bariatric surgery may prolong recovery time. Most morbidly obese patients have obstructive sleep apnea and cardiac comorbidities. In these patients, prolonged postoperative pain may cause early ambulation and delay performing deep breathing exercises.

Using regional anesthetic techniques results in less opioid use and better pain management. External oblique internal costal block; It is a new block that provides dermatomal sensory blockage involving T6-T10 in the anterior axillary line and T6-T9 in the midline. It can be used as part of multimodal analgesia in laparoscopic cases.

There is no study in the literature regarding the use of external oblique plane block in bariatric surgery yet.

Registry
clinicaltrials.gov
Start Date
November 15, 2022
End Date
May 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ali Ahiskalioglu

Principal Investigator

Ataturk University

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

Postoperative opioid consumption

Time Frame: first 24 hours

First 24 hours total fentanyl consumption with patient controlled analgesia

Secondary Outcomes

  • Visual analog pain score(postextubation 0-24 hours)

Study Sites (1)

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