Which liver biopsy needle delivers the best tissue? a Head-to-Head comparison
NCT ID NCT07701031
First seen Jul 14, 2026 · Last updated Jul 16, 2026 · Updated 2 times
Summary
This study compares different ways to take a liver biopsy in adults with chronic liver disease, cirrhosis, or who have had a liver transplant. The goal is to see which method—traditional percutaneous (through the belly) or endoscopic ultrasound-guided (through the stomach)—provides the best tissue sample for diagnosis and causes the least pain. Patients are assigned to one of five needle types in sequence, and researchers measure the length and quality of the tissue obtained, as well as any discomfort.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- liver biopsy performed with different needle types (EUS 19G FNA, 19G FNB, 22G FNA, 22G FNB, and percutaneous 18G Trucut)
- What this could lead to
- If one method proves superior, it could become the preferred technique for obtaining high-quality liver tissue samples with less pain.
- What could go wrong
- This is a single-center study with a small sample size, so results may not apply to all hospitals. The sequential design may introduce bias, and the optimal needle may still depend on patient factors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
146 people
The number who actually took part.
- Started
-
Jan 2023
- Finished
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Nov 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
All consecutive adult patients undergoing clinically indicated untargeted liver biopsy during the study period at our tertiary liver center.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * clinical indication for non-targeted liver biopsy * written informed consent Exclusion Criteria: * ascites * severe coagulopathy (INR \>2.0 or platelet count \<50 × 10³/µl) * contraindications to endoscopy or sedation * anatomical conditions precluding safe liver biopsy * pregnancy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University Hospital Muenster
Münster, 48149, Germany
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