Actively Recruiting
Genetics of Primary Graft Dysfunction Following Lung Transplantation
Led by University of Pennsylvania · Updated on 2025-07-16
1150
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Pennsylvania
Lead Sponsor
N
National Heart, Lung, and Blood Institute (NHLBI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Primary graft dysfunction (PGD) is a serious lung injury that can occur within days after lung transplant surgery. This condition affects up to 25% of lung transplant patients and is the leading cause of death after the procedure. Researchers are studying specific genetic factors in both lung donors and recipients that may increase the risk of developing PGD. Understanding these genetic markers could help predict who is more likely to experience this complication and potentially allow more transplants to be performed safely. The study involves individuals undergoing lung transplantation. Blood samples will be collected from lung donors and recipients before surgery, right after surgery, and 24 hours post-surgery. Researchers will monitor participants closely for 72 hours after surgery to check for symptoms of PGD, such as fluid buildup in the lungs and low blood oxygen levels. There are no additional study visits beyond this monitoring period. Participants will provide blood samples at specified times around their transplant surgery. During the first 72 hours after surgery, researchers will watch for signs of PGD to better understand its development in relation to genetic factors. This study does not require extra visits, focusing on the immediate post-surgery period. The main measurement is the presence or absence of primary graft dysfunction within 72 hours following the lung transplant.
CONDITIONS
Brief Title
Identifying Genetic Characteristics That Increase Risk of Primary Graft Dysfunction Following Lung Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Undergoing lung transplant surgery
You will not qualify if you...
- Individuals undergoing multi-organ transplantation except heart/lung transplants
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 3 days
Participants undergo lung transplant surgery. Blood samples are collected before surgery, immediately after surgery, and 24 hours after surgery. Participants are monitored for symptoms of primary graft dysfunction for 72 hours following surgery.
No additional study visits beyond surgery and monitoring period
Trial Site Locations
Total: 1 location
1
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0