Prospective Multicenter Research on Donor and Recipient Management Strategies to Improve Lung Transplant Outcomes
Start Date
9/3/2024
Completion Date
6/30/2027
Summary
This project aims to collect detailed clinical data, blood samples, and patient-reported outcomes from 2,600 lung transplant candidates, donors, and recipients at Lung Transplant Centers. The goal is to create a robust resource for various research objectives, including studying the impact of variations in donor and medical practices on clinical outcomes. The project also seeks to identify serum biomarkers associated with or predictive of specific post-transplant complications and conditions.
Detailed Description
This is an observational, prospective, multicenter cohort study of 2,600 lung transplant donors and adult (18 years and older) lung transplant candidates and recipients that will collect longitudinal clinical data, and serial biological (blood) specimens and PROs to support a broad range of clinical and translational future research. Data and biospecimens will be rigorously collected and monitored to ensure high quality future studies that will address unmet needs and optimal management at each stage of the transplant journey from listing, to donor selection, to postoperative management. Subjects are recruited to the study either prior to undergoing lung transplant at the time of listing or within 30 days of having undergone a lung transplant at one of the enrolling centers. The study design will generally follow the SOC practices at each center to minimize additional research related visits. Participants will follow the SOC transplant protocols at each site. Every attempt will be made by the site to collect study data and research specimens from participants at the time of SOC visits. Participation in this study will include scheduled data extraction or data transfers at specified time intervals, serial prospective blood collection (including plasma, serum), recipient DNA sample collection (with donor DNA sample collection optional), and PRO measures.
Eligibility Criteria
Age Range: 18 years to No maximum
Conditions
Locations
University of California Los Angeles
Los Angeles, California 90095
United States
University of California at San Francisco
San Francisco, California 94143
United States
Stanford University Medical Center
Stanford, California 94305
United States
University of Miami
Miami, Florida 33136
United States
Johns Hopkins University
Baltimore, Maryland 21205
United States
Brigham and Womens Hospital
Boston, Massachusetts 02115
United States
University of Michigan
Ann Arbor, Michigan 48109
United States
University of Minnesota
Minneapolis, Minnesota 55455
United States
New York University
New York, New York 10016
United States
Columbia University
New York, New York 10032
United States
Duke University Medical Center
Durham, North Carolina 27710
United States
University of Pennsylvania
Philadelphia, Pennsylvania 19104
United States
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania 15261
United States
Vanderbilt University Medical Center
Nashville, Tennessee 37232
United States
Houston Methodist Hospital, Texas Medical Center
Houston, Texas 77030
United States
Inova Fairfax Hospital
Falls Church, Virginia 22042
United States
University of Washington
Seattle, Washington 98109
United States
University of Wisconsin Hospital and Clinics
Madison, Wisconsin 53792
United States
University Health Network
Toronto,
Canada