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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03820271
Other study ID # K170914J
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2020
Est. completion date October 1, 2023

Study information

Verified date April 2022
Source Assistance Publique - Hôpitaux de Paris
Contact Christophe Duvoux, PHD
Phone 01 49 81 43 28
Email christophe.duvoux@aphp.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The MELD score is a predictive model of cirrhosis mortality used in France since 2007 to prioritize access to liver transplantation for patients enrolled in the national waiting list. The predictive value of this score was recently revised downward with a C index of the order of 0.65-0.67 and 20% of the patients enrolled for decompensated cirrhosis have access to liver transplantation by a subjective system of "expert component" independent of the MELD because of this lack of precision. The use of the MELD score to individually define access to the transplant should so be reconsidered. Recently new predictive models of cirrhosis mortality better than MELD have been developed and new mortality predictors independent of MELD have been published. The goal of this study is to design prognostic predictive models of mortality for decompensated cirrhotic patients enrolled on the national liver transplant waiting list including known (MELD, MELD Na) as more recent (CLIF-C AD, CLIF - CACLF) predictive models and new objective predictors studied in combination in order to optimize the system of allocation of hepatic allografts in France. The expected benefits of this search are twofold: - At the individual level: The possibility for patients at high risk of death but with intermediate MELD score to be transplanted. - Public health plan: - Improving the equity of graft allocation system. - Decreased mortality in the waiting list by improving the fairness and efficiency of the graft allocation system, a major public health issue


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date October 1, 2023
Est. primary completion date October 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients (=18 years old) newly registered on national waiting list with main diagnosis "cirrhosis" - Patients enrolled on the national waiting list under the "national liver score" allocation scheme whether an expert component is considered or not - Patients (or trusted person or family member or close relation if the patient is unable to express consent) who have been informed and signed their informed consent - Patients affiliated to a health insurance scheme Exclusion Criteria: - Patients enrolled with decompensated cirrhosis associated with hepatocellular carcinoma - Patients on AVK (INR and therefore MELD and CLIF scores uninterpretable) - Vulnerable population (person under guardianship or curatorship or deprived of liberty by a judicial decision) - Pregnant and / or breastfeeding woman

Study Design


Related Conditions & MeSH terms


Intervention

Other:
SuperMELD
The population of this arm will consist of patients newly enrolled in the National Liver Transplantation Waiting List for decompensated cirrhosis, whose liver function and MELD score are assessed at enrollment and then routinely reassessed at least quarterly during the waiting phase. Patients will be followed from their listing to transplantation or discharge or death.

Locations

Country Name City State
France Pr Duvoux Créteil

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary predictive value of the new multivariate prognostic models in patients listed for decompensated cirrhosis Predictive value of mortality and drop out in the waiting list Month 3.
Secondary Individual predictive value of each of the new candidate predictors CRP, copeptin, NT-pro BNP, vitamin D, leucocytes, PMN/lymphocytes ratio, urinary NGal, cystatin C, frailty index, sarcopenia (abdominal tomodensitometry to measure the surface of psoas), caloric intake, encephalopathy (ammonia level, stroop application), and transferrin. Month 3. Month 6, Month 9, Month 12Month 12
Secondary Complications predicted by each of the independent predictors infection, renal dysfunction, encephalopathy, bleeding, ACLF Month 3 Month 6, Month 9, Month 12.Month 12
Secondary Added predictive value for mortality and drop out of new multivariate prognostic models on MELD (model end stage for liver disease) Months 3, Month 6, Month 9, Month 12.
Secondary Evaluation of the predictive value of the CLIF (Chronic LIver Failure)-C (cirhosis) AD (Decompensation) score in decompensated cirrhotics listed without organ failure death and drop out Months 3, Month 6, Month 9, Month 12.
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