Registry of hospitalized patients with liver cirrhosis
Registry of Adult Consenting Patients Admitted to the Liver Unit With Liver Cirrhosis
This study is collecting information from adults hospitalized with liver cirrhosis to better understand their health outcomes and complications after they leave the hospital.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2000 (estimated) |
| Ages | 19 Years and up |
| Sex | All |
| Sponsor | F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica Academic / other |
| Locations | 1 site (Banská Bystrica) |
| Trial ID | NCT04767945 on ClinicalTrials.gov |
What this trial studies
This observational study collects data from adult patients hospitalized with liver cirrhosis at F.D. Roosevelt Teaching Hospital. Patients are offered participation upon admission, and their demographic, clinical, and laboratory data are recorded with their consent. After discharge, follow-up visits are encouraged, and mortality data is regularly updated from the national registry. The aim is to create a comprehensive registry to better understand the outcomes and complications associated with liver cirrhosis.
Who should consider this trial
Good fit: Ideal candidates are adults hospitalized with liver cirrhosis who experience a decompensating event.
Not a fit: Patients who decline to provide consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could improve the management and treatment of patients with liver cirrhosis by providing valuable insights into their health outcomes.
How similar studies have performed: While observational registries are common, this specific approach to tracking hospitalized cirrhosis patients is relatively novel and may provide unique insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * liver cirrhosis (primarily on clinical grounds) * decompensating event leading to hospital admission * informed consent Exclusion Criteria: * declined consent
Where this trial is running
Banská Bystrica
- F.D.Roosevelt Teaching Hospital — Banská Bystrica, Slovakia (Recruiting)
Study contacts
- Principal investigator: Lubomir Skladany, MD PhD — F.D.Roosevelt Teaching Hospital, Banska Bystrica, Slovakia
- Study coordinator: Lubomir Skladany, MD, PhD
- Email: lubomir.skladany@gmail.com
- Phone: +421905482997
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.