Prospective Multicenter Research on Donor and Recipient Management Strategies to Improve Lung Transplant Outcomes (NCT06399302)
Prospective Multicenter Research on Donor and Recipient Management Strategies to Improve Lung Transplant Outcomes: PROMISE-Lung Study
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: To join this study, participants generally need to meet the listed inclusion criteria (4 items) and avoid the listed exclusions (4 items).
Location: University of California Los Angeles — Los Angeles, California
Age range: 18 Years
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistCheck every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).
Usually NOT eligible if any of the following apply:
- Exclusion Criteria:
- Unwillingness of a participant or legally authorized representative (LAR) to give written informed consent or comply with study protocol
- Pregnancy or plans to become pregnant
- Past or current medical problems or findings from physical examination or laboratory testing, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.
🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.
📍 All Participating Trial Locations (19 Sites)
- University of California Los Angeles — Los Angeles, California
- University of California at San Francisco — San Francisco, California
- Stanford University Medical Center — Stanford, California
- University of Miami — Miami, Florida
- Johns Hopkins University — Baltimore, Maryland
- Brigham and Womens Hospital — Boston, Massachusetts
- University of Michigan — Ann Arbor, Michigan
- University of Minnesota — Minneapolis, Minnesota
- New York University — New York, New York
- Columbia University — New York, New York
- Duke University Medical Center — Durham, North Carolina
- University of Pennsylvania — Philadelphia, Pennsylvania
- University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania
- Vanderbilt University Medical Center — Nashville, Tennessee
- Houston Methodist Hospital, Texas Medical Center — Houston, Texas
- Inova Fairfax Hospital — Falls Church, Virginia
- University of Washington — Seattle, Washington
- University of Wisconsin Hospital and Clinics — Madison, Wisconsin
- University Health Network — Toronto, Canada
📞 Contact the Study Coordinator
Phone: (919) 259-4414
Email: allyn.damman@duke.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Lung Transplant; Complications
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- Inspiratory Work of Breathing Before and After Extubation — Toronto, Ontario
- Early Use of Long-acting Tacrolimus in Lung Transplant Recipients — Nashville, Tennessee
Explore by condition: All Lung Transplant; Complications clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.