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

I

Institute of Liver and Biliary Sciences, India

Status

Enrolling

Conditions

Liver Cirrhosis

Treatments

Other: Liver Disease of all etiologies

Study type

Observational

Funder types

Other

Identifiers

NCT06469489
ILBS-SAFE-TJLB

Details and patient eligibility

About

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.

Full 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).

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 18-65 years age.
  2. Patient with suspected or known liver disease undergoing trans-jugular liver biopsy as per clinical indication.

Exclusion criteria

  • None

Trial design

60 participants in 1 patient group

Liver Disease patients undergoing Trans-Jugular Liver Biopsy
Treatment:
Other: Liver Disease of all etiologies

Trial contacts and locations

1

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Central trial contact

Dr Satender Pal Singh, DM

Data sourced from clinicaltrials.gov

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