Toronto EVLP System™
DeviceExtending preservation and assessment time of donor lungs using the Toronto EVLP System
NCT Number: NCT02234128
This is a safety study to compare the safety of receiving a lung treated with the Toronto EVLP System™ by SPONSOR in SPONSOR's dedicated facility against standard lung transplantation.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Mayo Clinic Jacksonville, Jacksonville, Florida, United States
Human donor lungs allocated to a participating study transplant center (Study Center) for a specific recipient and meeting study EVLP donor lung inclusion/exclusion criteria will be assessed by SPONSOR for inclusion into the study.
Upon retrieval, donor lung(s) will be packaged and transported on ice to the SPONSOR's EVLP facility in Silver Spring, Maryland, no differently than when lungs are recovered, packaged, and transported to any transplant center for implantation.
The EVLP procedure will be performed by Certified Ex Vivo Lung Specialists using the Toronto EVLP System™ for up to 6 hours, collecting and relaying lung function assessment data hourly or as requested by the Study Center transplant surgeon. Additionally, the Study Center surgeon will have the capability to evaluate lung function data and monitor the procedure remotely through a dedicated video link.
Upon acceptance of an EVLP donor lung by the Study Center, the single lung or lung block is cooled down by the Toronto EVLP System™ to 10 degrees C. Thereafter, perfusion and ventilation are stopped and the lung is prepared for hypothermic storage and transport to the accepting Study Center.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Subject Inclusion Criteria:
In order to be eligible to participate in this study, an individual must meet all of the following criteria:
Subject Exclusion Criteria:
A subject who meets any of the following criteria will be excluded from participation:
Donor Lung Inclusion Criteria for EVLP Assessment:
The donor lung must meet at least one of the following criteria to proceed with EVLP:
Donor Lung Exclusion Criteria for EVLP Assessment:
The donor lung is excluded from EVLP if at least one of the following criteria have been met:
EVLP Lung Inclusion Criteria for Transplantation:
The donor lung must meet each of the following conditions post-EVLP for transplant suitability consideration by the Study Center Investigator:
EVLP Lung Exclusion Criteria for Transplantation:
The donor lung is excluded from transplant inclusion if at least one of the following criteria have been met:
Extending preservation and assessment time of donor lungs using the Toronto EVLP System
Time frame: 72 Hours
Primary Graft Dysfunction is a scale published by the International Society of Heart and Lung Transplantation that uses patient oxygenation and radiographic results to score patients on a 0 (zero) to 3 (three) scale, with 3 being the most significant dysfunction.
Time frame: 30 Days
The number of participants that survived to 30 days post-transplant.
Time frame: 0, 24, 48 & 72 Hours
Primary Graft Dysfunction is a scale published by the International Society of Heart and Lung Transplantation that uses patient oxygenation and radiographic results to score patients on a 0 (zero) to 3 (three) scale, with 3 being the most significant dysfunction. PGD Score (0-3) was determined at 0, 24, 48 & 72 hours post-transplant
Time frame: One year
Number of days in Intensive Care Unit post transplant.
Time frame: 72 Hours
Time in hours between cross-clamp in donor and reperfusion in recipient.
Time frame: One year
Number of hours from admission to ICU post-transplant to extubation of the participant.
Time frame: One year
Duration of primary hospital stay in days.
Lung Bioengineering Inc.
Industry
A Phase 2, Multicenter, Open-label Study to Measure the Safety of Extending Preservation and Assessment Time of Donor Lungs Using Normothermic Ex Vivo Lung Perfusion and Ventilation (EVLP) as Administered by the SPONSOR Using the Toronto EVLP System™
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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