Clinical trial

Evaluation of the Safety and Performance of Perla® Preservation Solution for Donor Liver and Kidney for Transplantation

Name
CIP001A
Description
Perla® is a Cold Preservation Solution, with purpose to wash out, preserve during transport liver and kidney grafts in optimal conditions from the donor to the recipient. The purpose of the PERTRIAL clinical investigation is to demonstrate the Performance and Safety of Perla® Cold Preservation solution.
Trial arms
Trial start
2021-12-11
Estimated PCD
2022-04-30
Trial end
2022-04-30
Status
Completed
Treatment
Perla® Cold Preservation solution
Perla® must be cooled to 2° to 6 °C prior to use. The cold Preservation Solution is used to flush the isolated organ immediately before removal from the donor and/or immediately after removal from the donor. The solution is then left in the organ vasculature during hypothermic storage and transportation.
Arms:
Perla® Cold Preservation solution
Size
11
Primary endpoint
Graft Function Rate (Kidney & Liver)
7 days post transplant
Eligibility criteria
Donor kidney / liver eligibility criteria: Inclusion Criteria: * Donor kidney / liver suitable for preservation * Donor age equal or over 18 years old * Donor meets one of the following conditions: * Donor after brain death (DBD), standard and extended criteria (SCD \& ECD) * Donor after circulatory death (DCD), cardiac arrest Maastricht classification III (awaiting cardiac arrest, controlled) Exclusion Criteria: * Donor participating at the same time in another Clinical Investigation Recipient eligibility criteria: Inclusion Criteria: * Patient registered primary kidney or liver transplant candidate, male or female * Patient ages ≥ 18 years old * Patient who has signed written informed consent Exclusion criteria: Patient recipient will not be included if any of the following conditions exists: * Prior solid organ or bone marrow transplant * Multi-organ transplant * Contraindications to transplantation (Active infection, active malignancy, pregnant females, females intending to get pregnant, or not willing to use a secure contraceptive method) * Participation in another clinical trial * Patient unable to give consent
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 11, 'type': 'ACTUAL'}}
Updated at
2023-05-17

1 organization

1 product

2 indications