University Hospital Bonn
Bonn, Germany
NCT Number: NCT03628807
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.
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Notify Me18 year–100 year
All sexes
Observational
Bonn, Germany
NEPTUN consists of liver cirrhosis receiving transjugular intrahepatic portosystemic shunt (TIPS) at the Department of Internal Medicine I, University of Bonn, Germany and receiving a structured routine evaluation and follow up program. The diagnosis of cirrhosis was based on clinical, hemodynamic and biochemical parameters, and ultrasound and/or biopsy criteria.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: up to 10 years
death, liver transplantation
Time frame: up to 10 years
Evaluation of amount of ascites according to the Child-Score
Time frame: up to 10 years
Evaluation of the grade according to the West Haven Criteria
Time frame: up to 10 years
Assessment of presence of variceal bleeding
Time frame: up to 10 years
defined as Bilirubin level ≥ 12mg/dl
Time frame: up to 10 years
Presence of ACLF according to the EASL-Chronic liver Failure Consortium (CLIF)-criteria
Time frame: up to 10 years
Assessment of Organ failures according to the CLIF-SOFA
according to CLIF-Sequential Organ Failure Assessment (SOFA) Score
University Hospital, Bonn
Other
Non-invasive Evaluation of Prognostic Parameters for Patients With Transjugular Intrahepatic Portosystemic Shunt (TIPS) Using a Structured Follow up Protocol
Acronym: NEPTUN
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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