Transjugular Intrahepatic Portosystemic Shunt (TIPS) for the Treatment of Portal Hypertension: an Observational Study

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

Patients with clinically significant portal hypertension allocated to implantation of a transjugular intrahepatic portosystemic shunt (TIPS) at the Department of Medicine II of the University Medical Center Freiburg, Germany will be offered to participate in this prospective observational trial. Clinical and laboratory as well as outcome parameters will be assessed before and within the first 12 months after TIPS implantation following a regular follow-up schedule with clinical visits at the University Medical Center Freiburg. During follow-up visits, serum/plasma samples and peripheral blood mononuclear cells (PBMC) are collected and stored in a associated biobank.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• Patients allocated to TIPS implantation due to clinically significant cirrhotic and non-cirrhotic portal hypertension

Locations
Other Locations
Germany
University Medical Center Freiburg, Department of Medicine II
RECRUITING
Freiburg Im Breisgau
Contact Information
Primary
Dominik Bettinger, MD
dominik.bettinger@uniklinik-freiburg.de
49761270-36870
Time Frame
Start Date: 2023-01-01
Estimated Completion Date: 2034-06-30
Participants
Target number of participants: 2000
Treatments
Patients allocated to implantation of a transjugular intrahepatic portosystemic shunt (TIPS)
Patients allocated to implantation of a transjugular intrahepatic portosystemic shunt (TIPS) due to cirrhotic and non-cirrhotic portal hypertension
Sponsors
Leads: University Hospital Freiburg

This content was sourced from clinicaltrials.gov