CompletedNot Applicable

Recto-intercostal Facial Plane Block in Laparoscopic Hiatus Hernia Repair

Egypt44 participantsStarted 2025-02-17

Plain-language summary

The aim of this study is to evaluate the perioperative analgesic and intraoperative hemodynamic effects of ultrasound-guided bilateral recto-intercostal fascial plane block in patients undergoing laparoscopic Hiatus hernia repair.

Who can participate

Age range18 Years – 65 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age from 18 to 65 years. * American Society of Anesthesiology (ASA) physical status I-II. * Both sexes. * Type 1 hiatus hernia (sliding hiatus hernia) with gastro-esophageal reflux disease and scheduled for elective laparoscopic hiatus hernia repair under general anesthesia. Exclusion Criteria: * Patients with cardiovascular, pulmonary, or neurological diseases. * History of chronic pain or Long-term or recent use of opioids. * Coagulation disorders or infection at the block application area. * History of allergy to local anesthetic drugs. * History of previous abdominal surgery. * Pregnancy. * Patients with gastro-esophageal reflux disease complicated by high grade esophagitis, esophageal stenosis or bleeding, and aspiration pneumonia or asthma.

What they're measuring

Total postoperative opioid consumption in the first 24 hours after surgery.

Timeframe: 24 hours after surgery.

Trial details

NCT IDNCT06820216

SponsorTanta University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-08-20

View on ClinicalTrials.gov More Rectointercostal trials