Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06621472

Retrolaminar Block Versus Subcostal Transversus Abdominis Plane Block in Liver Resection Surgery

Led by Cairo University · Updated on 2026-03-18

90

Participants Needed

1

Research Sites

86 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Adequate pain control improves postoperative outcomes and is imperative for enhanced recovery after surgery (ERAS) . Open liver resection surgery is associated with intraoperative blood loss, hypotension, coagulopathy, pulmonary complications, liver impairment, and renal impairment, making perioperative pain management challenging . Multimodal analgesic strategies employing regional techniques decrease postoperative pain and opioid consumption following liver resections. Thoracic epidural analgesia (TEA) is considered the 'gold standard' for open thoracic and abdominal surgical procedures .

CONDITIONS

Official Title

Retrolaminar Block Versus Subcostal Transversus Abdominis Plane Block in Liver Resection Surgery

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Physical status American Society of Anesthesiologists (ASA) II or III
  • Body mass index (BMI) between 20 and 35 kg/m2
Not Eligible

You will not qualify if you...

  • Patient refusal to participate
  • Physical status ASA IV
  • Body mass index (BMI) less than 20 kg/m2 or greater than 35 kg/m2
  • Known sensitivity or contraindication to local anesthetics or opioids
  • History of psychological disorders or chronic pain
  • Contraindications to regional anesthesia such as local infection, existing peripheral neuropathies, or blood clotting problems
  • Severe respiratory, cardiac, or kidney disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cairo University

Cairo, Egypt, 11835

Actively Recruiting

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Research Team

S

sayed M abed, MD degree

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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