EUS Guided Portal-systemic Pressure Gradient Measurement
Recruiting
Phase 1
Phase 2
Interventional Study
Portal Hypertension
Cirrhosis
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 75
- Sex
- Any
- Trial phase
- Phase 1/2
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 30 (estimated)
- Sponsor
- Chinese University of Hong Kong · Other
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About This Trial
Portal hypertension is characterised by an increased portal pressure gradient (PPG), that is the difference in pressure between the portal vein and the inferior vena cava (IVC). Portal hypertension is a consequence of cirrhosis resulting from chronic hepatitis. Patients with portal hypertension are at risk of developing complications including oesophageal or gastric varices, variceal bleeding, asc…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Suffering from chronic hepatitis induced cirrhosis
* Informed consent available
Exclusion Criteria:
* Medical
* Child-Pugh Class C
* Uncorrected platelet count \<50,000
* INR \> 1.5 (natural)
* Anatomical
* Previous transjugular intrahepatic or surgical portosystemic shunt
*…
Contacts