Safety and Adequacy of Trans-jugular Liver Biopsy in Patients With Liver Disease: SAFE-TJLB Study

Last updated: July 4, 2024
Sponsor: Institute of Liver and Biliary Sciences, India
Overall Status: Active - Recruiting

Phase

N/A

Condition

Primary Biliary Cholangitis

Hyponatremia

Hepatic Fibrosis

Treatment

Liver Disease of all etiologies

Clinical Study ID

NCT06469489
ILBS-SAFE-TJLB
  • Ages 18-65
  • All Genders

Study Summary

Liver biopsy is considered the gold standard for the evaluation of acute and chronic liver disorders. Liver biopsy provides information regarding diagnosis, disease progression, and response to therapy in patients with chronic liver diseases. Trans-jugular liver biopsy (TJLB) consists of obtaining liver tissue through a rigid cannula introduced into one of the hepatic veins typically using jugular venous access. This approach reduces the risk of hemorrhage after biopsy because the bleeding resulting from the biopsy needle will drain into the hepatic veins. In the past, the specimens obtained by a transjugular approach were considered suboptimal compared with the samples obtained with percutaneous needles because they were smaller and more fragmented. TJLB was initially indicated for patients who had a contraindication to percutaneous biopsy such as those with a coagulopathy or congenital clotting disorders, ascites, acute liver failure, large amount of adipose tissue, and patients after liver transplantation. The clinical role of TJLB has expanded due to the possibility of performing hemodynamic evaluation of the hepatic and portal venous systems, which provides useful information and may guide therapy in patients with portal hypertension.

Lacuna in literature:

There is no prospective study in India evaluating the safety and efficacy of trans-jugular liver biopsy in patients with liver disease.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. 18-65 years age.

  2. Patient with suspected or known liver disease undergoing trans-jugular liver biopsyas per clinical indication.

Exclusion

Exclusion Criteria:

  • None

Study Design

Total Participants: 60
Treatment Group(s): 1
Primary Treatment: Liver Disease of all etiologies
Phase:
Study Start date:
June 21, 2024
Estimated Completion Date:
September 30, 2024

Study Description

Hypothesis:

Trans-jugular liver biopsy is safe, gives adequate sample for pathological examination in patients with liver disease.

Aim of study:

To evaluate safety and adequacy of trans-jugular liver biopsy in patient with liver disease.

Primary objective:

  1. Adequacy of trans-jugular liver biopsy

  2. Safety of trans-jugular liver biopsy

Secondary objective:

  1. Indications of liver biopsy

  2. Procedural time (in and out of catheter)

  3. Number of passes

  4. Failure rate

  5. Day care time

  6. VAS: pain (Abdomen and Neck, pre and post procedure)

  7. Complications- arrythmia, hematoma

  8. Time of Fluro exposure

Patients and methods Study Design A prospective, observational cohort study will be conducted in patients with suspected or known liver disease between November 2023 to May 2024 at the Institute of Liver and Biliary Sciences (ILBS), New Delhi.

Clinical protocol An informed consent was taken from patients with liver disease undergoing liver biopsy as per clinical indication. The following demographic data was recorded at inclusion: Age, gender, co-morbidities, type, and etiology of liver disease. Laboratory parameters include complete blood count, liver function tests, kidney function tests, INR. Severity of liver disease (MELD score, CTP score, AARC score).

Connect with a study center

  • Institute of Liver & Biliary Sciences

    New Delhi, Delhi 110070
    India

    Active - Recruiting

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