Hepatectomy Clinical Trials

Clinical trials related to Hepatectomy Procedure

Comparison of Postoperative Analgesic Efficacy Between Erector Spinae Plane Block and Thoracic Epidural Analgesia in Open Hepatectomy: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Background: Open liver resection is associated with severe postoperative pain. While thoracic epidural analgesia (TEA) is considered the gold standard for pain control, its clinical application is often limited by postoperative coagulation profile derangement, which increases the risk of epidural hematoma. Continuous erector spinae plane block (ESPB) has emerged as a promising, safer alternative with a lower risk of bleeding complications.

Objective: This study aims to compare the postoperative analgesic efficacy, safety profiles, and impacts on respiratory function between ultrasound-guided continuous ESPB and TEA in patients undergoing elective open liver resection. Hypothesis: The investigators hypothesize that continuous ESPB using a programmed intermittent bolus (PIB) regimen is non-inferior to TEA regarding 72-hour postoperative pain scores at rest, while offering superior hemodynamic stability and fewer technique-related risks.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• \* Patients aged between 18 and 80 years old.

‣ American Society of Anesthesiologists (ASA) physical status classification I to III.

⁃ Scheduled to undergo elective open liver resection (open hepatectomy).

⁃ Patient provides written informed consent to participate in the study.

Locations
Other Locations
Viet Nam
Department of Anesthesiology and Resuscitation, Bach Mai Hospital
RECRUITING
Hà Nội
Time Frame
Start Date: 2026-01-01
Estimated Completion Date: 2026-07-01
Participants
Target number of participants: 60
Treatments
Active_comparator: Erector Spinae Plane Block Group
Patients will receive ultrasound-guided continuous bilateral erector spinae plane block at the T7 level with a programmed intermittent bolus (PIB) regimen of Ropivacaine 0.1% (18 mL/3h on the right side and 18 mL/3h on the left side) for 72 hours postoperatively, combined with systemic multimodal analgesia
Active_comparator: Thoracic Epidural Analgesia Group
Patients will receive a thoracic epidural catheter inserted at the T7-T8 interspace with a continuous basal infusion of Ropivacaine 0.1% at a rate of 5-8 mL/h for 72 hours postoperatively, combined with systemic multimodal analgesia
Sponsors
Leads: Nguyen Toan Thang

This content was sourced from clinicaltrials.gov