Actively Recruiting
Blood Group A2 Donor to Blood Group O Recipient Lung Transplantation
Led by University Health Network, Toronto · Updated on 2025-02-06
10
Participants Needed
1
Research Sites
365 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the safety and feasibility of lung transplants from blood group A2 donors to blood group O recipients. This study aims to increase the donor pool for blood group O lung transplant candidates, who often face longer wait times and higher mortality on the waitlist. It is the first prospective study worldwide to assess ABO-incompatible lung transplants in this way. The intervention involves lung transplant surgery using lungs from blood group A2 donors transplanted into blood group O recipients who have low anti-A antibody levels and a negative virtual crossmatch at the time of transplant. The study monitors the recipients closely after surgery to assess immune response and transplant success. Participants will be monitored through various evaluations including antibody levels on post-operative days 5 or 12, primary graft dysfunction grading in the first three days, and assessment for rejection or infection over the following years. Long-term follow-up up to 10 years will evaluate graft function, chronic lung problems, infections, malignancies, and survival outcomes. The total participation time varies depending on individual follow-up and outcomes.
CONDITIONS
Brief Title
A2 to O Lung Transplants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- First lung transplant
- Blood group O recipient
- Low pre-operative anti-A antibody titers
- Consent to study participation
You will not qualify if you...
- Previous lung transplant (re-transplant)
- Multiorgan transplant
- Positive virtual crossmatch at time of transplant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 1 week
Participants undergo lung transplant surgery from a blood group A2 donor to a blood group O recipient and receive immediate post-operative care.
Daily visits during post-op days 0 to 7
Duration - Up to 10 years
Participants are monitored for graft function, rejection, infection, and other health outcomes after surgery.
Scheduled visits at post-op day 12, 1 year, and periodic visits up to 10 years
Trial Site Locations
Total: 1 location
1
Toronto General Hospital, University Health Network
Toronto, Ontario, Canada, M5G 2C4
Actively Recruiting
Research Team
S
Sharaniyaa Balachandran
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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