Non-invasive evaluation for patients with portal hypertension receiving TIPS
Non-invasive Evaluation of Prognostic Parameters for Patients With Transjugular Intrahepatic Portosystemic Shunt (TIPS) Using a Structured Follow up Protocol 2
This study is testing new ways to monitor patients with portal hypertension who are getting a TIPS procedure to see how well they do afterward.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | University Hospital, Bonn Academic / other |
| Locations | 1 site (Bonn) |
| Trial ID | NCT04393519 on ClinicalTrials.gov |
What this trial studies
This program evaluates non-invasive prognostic parameters in patients undergoing transjugular intrahepatic portosystemic shunt (TIPS) due to complications from portal hypertension. Patients will be monitored through a structured follow-up program at the University Hospital Bonn, where clinical and laboratory data will be collected and analyzed for their prognostic value. The study aims to enhance understanding of patient outcomes following TIPS procedures using advanced imaging techniques such as echocardiography, CT scans, and MRIs.
Who should consider this trial
Good fit: Ideal candidates are patients with liver cirrhosis who are eligible for TIPS insertion according to established guidelines.
Not a fit: Patients with contraindications for TIPS will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the management and outcomes of patients with portal hypertension undergoing TIPS.
How similar studies have performed: While there have been studies on TIPS, this specific non-invasive evaluation approach is novel and may provide new insights into patient management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Insertion of TIPS according to guidelines Exclusion Criteria: * Contraindication for TIPS
Where this trial is running
Bonn
- University Hospital Bonn — Bonn, Germany (Recruiting)
Study contacts
- Principal investigator: Michael Praktiknjo, MD — University of Bonn
- Study coordinator: Michael Praktiknjo, MD
- Email: michael.praktiknjo@ukbonn.de
- Phone: +49(0)228-287 15770
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.