Non-Invasive Portal and Hepatic Vein Pressure Estimation
Recruiting
N/A
Interventional Study
Portal Hypertension
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 75
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 50 (estimated)
- Sponsor
- Leiden University Medical Center · Other
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About This Trial
Background Portal hypertension (PH) is a spectrum of complications of end-stage liver disease (ESLD) and cirrhosis, with severe manifestations including ascites and gastroesophageal varices. It is therefore important that timely and easily diagnosing PH has relevant prognostic and therapeutic implications. The current gold standard to evaluate PH is by hepatic vein catheterization using the transj…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Eligible for liver transplantation (LT) screening (which excludes pregnancy).
* Age ≥ 18 years and ≤ 75 (since \>75 is a contraindication for LT).
* Written informed consent.
Exclusion Criteria:
* Exclusion criteria for MRI (claustrophobia, pacemaker, metal implants, etc.).
…
Contacts