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Clinical Trials in Egypt / NCT07276646
Recruiting Not applicable

Perioperative Opioid-sparing Effect of Retrosuperior Costotransverse Ligament Block Versus Erector Spinae Block in Laparoscopic Cholecystectomy

NCT07276646 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-12-10
Last updated
2025-12-12

Condition(s) studied

Perioperative Analgesia

Investigational drug(s) / intervention(s)

Retrosuperior costotransverse ligament block groupErector spinae block group

Retrosuperior costotransverse ligament block group: The patient will receive retrosuperior costotransverse ligament block

Erector spinae block group: The patient will receive erector spinae block.

Study summary

This study aims to compare the analgesic effect of retro superior costotransverse ligament space block vs erector spinae plane block to Achieve high-quality perioperative opioid-sparing effect and postoperative analgesia after laparoscopic cholecystectomy with optimum hemodynamic stability and high patient and surgeon satisfaction

Eligibility

Sex
ALL
Min age
21 Years
Max age
64 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. patient acceptance 2. Age: 21-64 years old. 3. Sex: both sexes. 4. Physical status: ASA I \& II. 5. Body mass index (BMI): 18.5 - 30 kg/m2. 6. Type of operations: elective laparoscopic cholecystectomy. 7. Duration of surgery not more than 2 hours. Exclusion Criteria: 1. Known hypersensitivity to lidocaine or bupivacaine. 2. Patients with respiratory insufficiency. 3. Coagulation disorders or taking drugs affect surgical hemostasis. 7\. Patients with pre-existing neurological deficits. 8. Uncooperative patient or with altered mental status. 9. Patient with advanced cardiovascular or respiratory diseases

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of human medicine, Zagazig university, Zagazig Zagazig Egypt Recruiting

More Zagazig University trials in Egypt

Other trials for the same condition

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 NCT07276646 on ClinicalTrials.gov ↗ ← All trials in Egypt