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Data Collection Study From Donors and Recipients to Optimize Donor-recipient Matching in Liver Transplantation

Optimizing Donor-recipient Matching to Improve Survival After Registration on the Waiting List for Liver Transplantation: the OPTIMATCH LT Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03371264
Acronym
OPTIMATCH-LT
Enrollment
9000
Registered
2017-12-13
Start date
2015-01-01
Completion date
2020-01-01
Last updated
2020-12-14

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

Conditions

Liver Transplantation

Keywords

Liver transplantation, Allocation process, Extended-criteria donors, Survival

Brief summary

A major limitation of liver transplantation is organ shortage. To avoid exposing patients to death on the waiting list, organs are used that would have been discarded few years ago. Graft allocation is regulated by the agence de biomedecine which establishes a national score. Each liver graft is proposed to the patient presenting the higher score. Acceptance or rejection of the graft only depends on the decision of each centre. We propose to submit a more efficient allocation model (enabling each proposed liver graft to be transplanted in the candidate whose transplantation will afford the greatest survival benefit after registration), by collecting and analysing variables from donors and candidates/recipients.

Interventions

None listed

Sponsors

Agence de La Biomédecine
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Liver transplant candidates : All adult LT candidates listed on the French wait list between 2009 and 2014 and followed prospectively by the mean yearly follow-up under the control of ABM. * Donors : all adults donors registered over the same 2009-2014 period, including donors whose livers were procured and transplanted, whose liver were procured and discarded, and donors in whom liver was not harvested.

Exclusion criteria

* Pediatric recipients * Pediatric donors

Design outcomes

Primary

MeasureTime frameDescription
Survival analysis5 yearsIn view of the complexity of our project, different parallel approaches will be performed in order to establish predictive models
Multi-state models5 yearsIn view of the complexity of our project, different parallel approaches will be performed in order to establish predictive models
Decision tree analysis5 yearsIn view of the complexity of our project, different parallel approaches will be performed in order to establish predictive models

Secondary

MeasureTime frameDescription
Percentage of each criterion of ECD (Donor population)5 years
Donor scores (DRI, ELTR) (Donor population)5 years
mean score (Donor population)5 years
mean age of donors (Donor population)5 years
graft failure (Donor population)5 years
grafts with correct primary function (Donor population)5 years
epidemiological characteristics (Candidate population)5 years
indication for transplantation (Candidate population)5 years
number of ECD criteria (Donor population)5 years
comorbidities (Candidate population)5 years
time on waiting list (Candidate population)5 years
Proportion of early deaths after transplantation (Candidate population)5 years
drop-outs for worsening (Candidate population)5 yearsDescription of events occurring on waiting list
deaths on the waiting list (Candidate population)5 years
median time of occurrence (Candidate population)5 yearsDescription of events occurring on waiting list
number of drop-outs for improvement (Candidate population)5 years
percentages of drop-outs for improvement (Candidate population)5 years
severity of disease (Candidate population)5 years
frequency of ECD criteria (Donor population)5 years
Number of each criterion of ECD (Donor population)5 years

Outcome results

None listed

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