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Clinical Trial Summary

Continued Access Protocol to evaluate the effectiveness of the OCS Liver System to preserve and assess donor livers.


Clinical Trial Description

A prospective, single arm, continued access protocol to evaluate the effectiveness of the OCS Liver System to preserve and assess donor livers having one or more of the following characteristics: 1. Donor age equal to or greater than 40 years old, or 2. Expected cross clamp time of 6 hours or greater, or 3. Donor after circulatory death (DCD) with age less than or equal to 55 years; or 4. Steatotic lever >0% and less than or equal to 40% at time of retrieval, based on pre-retrieval histology) A maximum of 21 sites will enroll up to 184 transplanted liver recipients. The primary effectiveness endpoint will be the incidence of Early Allograft Dysfunction (EAD) or primary non-function. All recipients will be followed for 24 months from the date of transplantation (some of which will be post-market). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04186221
Study type Interventional
Source TransMedics
Contact
Status Completed
Phase N/A
Start date February 3, 2020
Completion date February 2, 2023

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