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RecruitingNCT07233083

External Oblique Intercostal Plane Block for Liver Transplantation Recipient

External Oblique Intercostal Plane Block for Postoperative Analgesia in Liver Transplantation

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Istinye University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Postoperative pain management is one of the key factors in improving rehabilitation and accelerating recovery. The external oblique intercostal plane block can be used to provide abdominal wall analgesia for effective pain control in abdominal surgery. The aim of this study is to investigate the postoperative analgesic efficacy of the external oblique intercostal plane block in liver transplant recipients. The investigators will compare a group receiving the external oblique intercostal plane block with a control group to determine whether this block provides effective postoperative analgesia in liver transplant recipients.

Detailed description

Patients scheduled for liver transplantation will be separated into 2 groups: External Oblique Intercostal Plane Block Group and Control Group. Patients in the External Oblique Intercostal Plane Block Group will be performed bilateral External Oblique Intercostal Plane Block at the end of the surgery and after skin closure and will receive patient controlled analgesia with morphine for postoperative analgesia. Patients in the Control Group will not receive any block procedure and will receive patient controlled analgesia with morphine for postoperative analgesia. Morphine consumption for first postoperative 48 hours, visual analog scale scores, time to need for first rescue analgesia, amount of rescue analgesic drug, incidence of postoperative nausea and vomiting, and Quality of Recovery-15 scores will be recorded.

Conditions

Interventions

TypeNameDescription
OTHERExternal Oblique Intercostal Plane BlockExternal oblique intercostal plane block will be administered at the end of the surgery and after skin closure
OTHERSham ProcedureSham Block (Ultrasound probe placement without needle insertion or injection)

Timeline

Start date
2025-12-22
Primary completion
2026-05-01
Completion
2026-06-01
First posted
2025-11-18
Last updated
2026-01-08

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07233083. Inclusion in this directory is not an endorsement.