RecruitingNot ApplicableNCT07233096

Rectus-Intercostal Fascial Plane Block for Liver Transplantation Donors

Evaluation of Postoperative Analgesic Efficacy of Ultrasound-Guided Rectus-Intercostal Fascial Plane Block in Living Liver Donors


Sponsor

Istinye University

Enrollment

64 participants

Start Date

Dec 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Postoperative pain control plays a crucial role in enhancing recovery and improving early mobilization in living liver donors. The rectus-intercostal fascial plane (RIFP) block is a novel ultrasound-guided regional anesthesia technique that provides anterior abdominal wall analgesia by targeting the intercostal nerves between the rectus abdominis and intercostal muscle fascia. This prospective, randomized controlled clinical study aims to evaluate the postoperative analgesic efficacy and opioid-sparing effects of the RIFP block compared with standard intravenous analgesia in living liver donors undergoing donor hepatectomy. Participants will be randomly assigned to two groups: Group 1 (RIFP Block): Patients receiving an ultrasound-guided rectus-intercostal fascial plane block using 20 mL of 0.25% bupivacaine at the end of surgery, in addition to standard IV PCA (morphine). Group 2 (Control): Patients receiving only standard IV PCA (morphine) without regional block.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria3

  • Age between 18 and 75 years
  • Patients with American Society of Anesthesiology (ASA) physical status I-II
  • Patients scheduled for a living donor hepatectomy

Exclusion Criteria7

  • Allergy to local anesthetics
  • Coagulopathy
  • Skin infection at the block area
  • Advanced renal failure
  • Chronic pain syndromes
  • Alcohol or drug abuse
  • Psychiatric disorders

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERRectus Intercostal Plane Block

Rectus intercostal plane block will be administered bilaterally at the end of the surgery and after skin closure under ultrasound guidance

OTHERControl (No Block)

Ultrasound probe placement on the same region without needle insertion or local anesthetic injection to maintain blinding.


Locations(1)

istinye University

Istanbul, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07233096


Related Trials