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Institutional Registry of Liver Transplantation

Institutional Registry of Liver Transplantation

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02839616
Acronym
IRLT
Enrollment
500
Registered
2016-07-21
Start date
2016-07-31
Completion date
2020-07-31
Last updated
2016-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinical Registry, Liver Transplantation

Brief summary

The Institutional Registry of Liver Transplantation is a system for data collection related to patients with liver disease who are possible candidates for liver transplantion. This tool was designed by a multidisciplinary team that includes hepatologists, surgeons, informatics and biostatisticians. It intends to collect the information from the clinical evaluation, physical examination, complementary diagnostic methods and laboratory data. The information is captured sistematically, following structured, standardized and monitored processess to ensure the quality of the data obtained. The aim is to use the available technology to generate a complete database that can be used to answer research questions.

Interventions

PROCEDUREorthotopic liver transplantation

Sponsors

Hospital El Cruce
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with indication for liver transplantation * Patients who are followed by the Liver Transplantation Unit of Hospital El Cruce

Exclusion criteria

* Patients who deny to participate after the informed consent process.

Design outcomes

Primary

MeasureTime frameDescription
Time to mortality5 yearsAll patients are followed from the date of the inclusion to the registry, by periodic controls by the hepatologists and through telephones calls by the coordinator nurse, both before and after the transplantation. Every patient who dies during the 5 years of follow up will count as an event. Patients who are lost to follow up will be censored, in this case we will use the date of the last control or telephone call where he or she was alive.

Secondary

MeasureTime frameDescription
Time to retransplantation5 yearsWe will considerate retransplantation as a competitive risk for death, calculating the time since the date of the transplant until the date of retransplantantion or not during the 5 years of follow up.

Countries

Argentina

Contacts

Primary ContactLiliana P Rojas Saunero, MD
palolili@gmail.com+54 11 4210 9000
Backup ContactFederico G Villamil, MD
fgvillamil@hotmail.com+54 11 4210 9000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026