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Clinical Trials in Egypt / NCT07311525
Recruiting Not applicable

Ultrasound-Guided RSCTL vs EOIP Block for Analgesia in Sleeve Gastrectomy

NCT07311525 · tracked via the Priya Life Science Egypt tracker
Sponsor
Beni-Suef University
Phase
Not applicable
Started
2026-02-01
Last updated
2026-01-06

Condition(s) studied

Patient Satisfaction

Investigational drug(s) / intervention(s)

ultrasound-guided Retro superior costotransverse ligament space blockultrasound-guided External Oblique Intercostal Plane Block

ultrasound-guided Retro superior costotransverse ligament space block: Participants will receive ultrasound-guided Retro superior costotransverse ligament space block after intubation. Following hydrodissection with 2 ml of 0.9% saline to confirm the correct needle tip position, 20 ml 0.25% bupivacaine was injected. The same procedure was then repeated with 20 ml 0.25% bupivacaine on the contralateral side.

ultrasound-guided External Oblique Intercostal Plane Block: Participants will receive ultrasound-guided External Oblique Intercostal Plane Block after intubation.Following hydrodissection with 2 ml of 0.9% saline to confirm the correct needle tip position, 20 ml 0.25% bupivacaine was injected. The same procedure was then repeated with 20 ml 0.25% bupivacaine on the contralateral side.

Study summary

The aim of this study is to compare the effect of ultrasound-guided retro-SCTL space block and EOI block on opioid consumption within 24 hours after LSG.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Patients aged between 18 to 65 years * Both genders * American Society of Anesthesiologists (ASA) physical status I-II * Body mass index (BMI) \> 40 kg m-2, Exclusion Criteria: * Obesity secondary to an endocrine disorder * known allergic diathesis to any drugs used in the study * Presence of serious systemic illness (e.g., severe cardiac, pulmonary, renal, or hepatic dysfunction), * Coagulation dysfunction * Pre-existing psychological disorders * Current use of analgesic or psychotropic medications * Infection at a potential injection site * Ahistory of chronic pain * Conversion to laparotomy.

Primary outcome measure(s)

  • cumulative morphine consumption within the first 24 hours. — 24 hours post operative
    cumulative morphine consumption within the first 24 hours.

Trial sites (1)

FacilityCityRegionStatus
Beni-Suef University hospital Banī Suwayf Beni Suweif Governorate Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07311525 on ClinicalTrials.gov ↗ ← All trials in Egypt