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NCT05101460

An All Comers Registry For Normothermic Ex Vivo Lung Perfusion (EVLP) as Assessment of Donor Lungs for Transplant

Recruiting now Last updated 14 July 2023
What this trial tests

trial testing XVIVO Perfusion System (XPS™) with STEEN Solution™ in Lung Transplant in 315 participants. Currently enrolling.

Timeline
29 October 2019
Primary endpoint
24 April 2024
24 April 2029

Quick facts

Lead sponsorXVIVO Perfusion
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment315
Start date29 October 2019
Primary completion24 April 2024
Estimated completion24 April 2029
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

XVIVO Perfusion — full company profile →

Who can join

18 and older, any sex, with Lung Transplant. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The XVIVO Registry is to collect standard of care clinical data from "all-comers" who are transplanted with an EVLP lung treated with the XVIVO Perfusion System™ in order to assess the long-term performance of the device, and monitor device-related serious adverse events. In addition, 4 and 5-year UNOS registry data of the 126 subjects who received an EVLP transplant under the NOVEL and NOVEL Extension studies are provided as part of the long-term safety and quality of life data. In addition, 4 and 5-year UNOS registry data of the 126 subjects who received an EVLP transplant under the NOVEL and NOVEL Extension studies are provided as part of the long-term safety and quality of life data.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Lung Transplant

Currently open trials in the same condition.

Other XVIVO Perfusion trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05101460.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing