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Austrian Registry on Transjugular Intrahepatic Portosystemic Shunts (AUTIPS)

T

Thomas Reiberger

Status

Enrolling

Conditions

Portal Hypertension

Treatments

Other: Observational study

Study type

Observational

Funder types

Other

Identifiers

NCT03409263
AUTIPS 1943/2017

Details and patient eligibility

About

Patients with TIPS will be recruited in this prospective registry study. The clinical course will be documented and biomarkers for prediction of complicatiosn will be assessed.

Full description

Patients with advanced chronic liver disease may develop portal hypertension, which is the main cause for most complications and deaths of patients with liver cirrhosis. Implantation of a transjugular intrahepatic portosystemic shunt (TIPS) leads to instantaneous alleviation of portal hypertension, but may cause hepatic encephalopathy. Stent grafts, as well as patient stratification and medical surveillance, have drastically improved over the past decades. However, there are few data on long-term outcome after TIPS implantation.This prospective registry study will assess the clinical course of patients after undergoing TIPS intervention and biomarkers for complications after TIPS implantation.

Enrollment

400 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-99 years
  • Portal hypertension
  • Anticipated or past implantation of a transjugular intrahepatic portosystemic shunt (TIPS)
  • Informed consent

Exclusion criteria

  • Retraction of consent

Trial contacts and locations

1

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Central trial contact

Thomas Reiberger, MD; Lukas Hartl, MD

Data sourced from clinicaltrials.gov

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