Extent of Sensory Blockade After External Oblique Intercostal Block for Postoperative Analgesia in Laparoscopic Sleeve Gastrectomy

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Drug
Study Type: Observational
SUMMARY

n obese patients, adequate pain relief in the postoperative period is a crucial parameter that affects patient comfort and hospital stay. Improving patient comfort and recovery quality can be achieved by minimizing undesirable effects such as nausea, vomiting, and inadequate analgesia. This study aimed to evaluate the impact of the external oblique intercostal block on postoperative dermatomal distribution, acute pain scores, and opioid consumption during the first 24 hours after laparoscopic sleeve gastrectomy surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 18-65 years

Locations
Other Locations
Turkey
Ondokuz Mayis University
RECRUITING
Samsun
Contact Information
Primary
Esra Turunc
esra.kiymaz.ek@gmail.com
+905074341884
Time Frame
Start Date: 2025-08-01
Estimated Completion Date: 2025-10-25
Participants
Target number of participants: 20
Treatments
Group EOIB
bilateral EOIB (60 ml, %0.25 bupivacaine, totally) + IV morphine patient-controlled analgesia (PCA)
Related Therapeutic Areas
Sponsors
Leads: Ondokuz Mayıs University

This content was sourced from clinicaltrials.gov

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