Non-invasive Evaluation Program for TIPS and Follow Up Network 2 (NEPTUN2)

Recruiting Observational Study
Portal Hypertension
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 100
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
University Hospital, Bonn · Other
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About This Trial

Evaluation of non-invasive prognostic parameters in patients receiving transjugular intrahepatic portosystemic shunt (TIPS) for complications of portal hypertension. Patients are cared according to the local standardized follow up program. Clinical and laboratory data from standard patient care are evaluated for potential prognostic value.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Insertion of TIPS according to guidelines Exclusion Criteria: * Contraindication for TIPS
Contacts

Michael Praktiknjo, MD

+49(0)228-287 15770

michael.praktiknjo@ukbonn.de

CONTACT

Johannes Chang, MD

+49(0)228-287 15770

johannes.chang@ukbonn.de

CONTACT