Evaluation and follow-up program for vascular liver diseases
Vascular Liver Disease Evaluation, Follow Up and Non-Invasive Diagnostics Program
This study looks at patients with vascular liver diseases to better understand their risk factors, treatment effects, and overall health outcomes over three years.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | University Hospital, Bonn Academic / other |
| Locations | 1 site (Bonn) |
| Trial ID | NCT03717792 on ClinicalTrials.gov |
What this trial studies
This program aims to improve understanding of vascular liver disorders (VALDI) by studying risk factors, diagnostic methods, treatment effects, and prognosis. Data will be collected from patients diagnosed with VALDI over a period of up to three years, focusing on clinical conditions, laboratory results, and outcomes. The study employs a standardized review of medical charts conducted by a specially trained investigator to ensure accurate and comprehensive data collection.
Who should consider this trial
Good fit: Ideal candidates for this program are patients diagnosed with vascular liver disease.
Not a fit: Patients without vascular liver disease will not benefit from this program.
Why it matters
Potential benefit: If successful, this program could lead to improved management recommendations for patients with vascular liver diseases.
How similar studies have performed: Previous studies on vascular liver disorders have been limited and retrospective, making this prospective observational approach novel and potentially impactful.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * all patients with vascular liver disease Exclusion Criteria: * patients without vascular liver disease
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: +4922828715770
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.