University Health Network, Toronto General Hospital
Toronto, Ontario, M5G 2C4, Canada
Location status: Recruiting
NCT Number: NCT07189377
The aim of the study is to show that transplantation of lungs from Hepatitis B-infected donors is safe when using EVLP with UV light inactivation plus antivirals
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 4
Toronto, Ontario, M5G 2C4, Canada
Location status: Recruiting
The success of transplantation is significantly hindered by the lack of sufficient available donors. Many potential donor organs are not fully utilized in clinical transplantation because donors have chronic viral infections. Currently, donors with chronic hepatitis B virus (HBV) infection are utilized by typically providing nucleoside analogues such as entecavir or lamivudine plus/minus several doses of HBIG. The entecavir or lamivudine are typically given either life-long in liver transplants or for 1 year in non-liver transplants. Donors with chronic HBV infection are Core Antibody positive (HBcAb +ve). These donors carry chronic virus but may be NAT positive or NAT negative. HBcAb+ve donors are routinely used, but NAT positive donors are typically not used. The Toronto lung transplant program commonly applies Ex Vivo Lung Perfusion (EVLP) to organs. This allows for treatment of organs prior to transplantation. The investigators have shown that UV light administered on the EVLP circuit can substantially decrease the amount of infectious virus. Such a strategy was previously employed with hepatitis C virus. The aim of the study is to show that transplantation of organs from HBV NAT+ve donors is safe with the use of UV light treatment on EVLP combined with post-transplant antivirals for the recipient (HBIG and entecavir). The investigators hypothesize that rates of HBV transmission to recipients will be prevented by the use of this approach and any HBV transmission that does occur will be readily treatable. This will be a small pilot study to determine the feasibility of this approach. If successful, the knowledge from this study can have an important impact on patients awaiting lung transplantation by providing a novel strategy for the use of HBV-positive organ donors, simplified through a shorter course of approved antivirals.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Donor Inclusion Criteria
Donor Exclusion Criteria
Recipient inclusion Criteria:
Recipient exclusion Criteria:
Recipients will receive 1mg administered orally, beginning pre-transplant as soon as the patient arrives to the hospital for surgery, and then 1mg post-operatively administered orally or via nasogastric tube once daily for 28 days.
Recipients will receive 4500 IU intravenously pre-transplant and then at day 3 and 7 post-transplant (3 doses total).
UV light therapy will be administered to the organ during EVLP prior to transplantation. For minimum 2 hours, maximum 6 hours (duration determined by time clinically required for EVLP based on standard clinical assessment of lung).
Time frame: At 6 months post-transplant
Participant blood samples will be taken at days 3 and 7, then weekly for the first 4 weeks, then every two weeks until 12 weeks post-transplant, then at month 6 after transplantation. Blood samples will be tested for HBV DNA via Nucleic Acid Amplification.
Time frame: From enrollment until 2 years post-transplant
Time frame: From enrollment until up to 2 years post-transplant
Time frame: From enrollment until 2 years post-transplant
Time frame: From time of infection until end of treatment or up to 2 years post-transplant
Time frame: From enrollment until 2 years post-transplant
Time frame: From enrollment until 2 years post-transplant
Time frame: From hospital admission until date of discharge or date of death from any cause, whichever comes first, assessed up to 2 years
Time frame: Measured 1 year post-transplant
Time frame: Measured 1 year post-transplant
Time frame: From enrollment until 2 years post-transplant
Contact information is provided by the study sponsor or research team.
University Health Network, Toronto
Other
Lung Transplantation Using Hepatitis B Positive Donors to Hepatitis B Negative Recipients Using Ex-Vivo Treatment of Organs: A Safety Trial
Acronym: CLEAR-HBV
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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