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NCT02904278
Pediatric Cardiac Transplantation, Pediatric Heart Transplant Recipients
Atlanta, Georgia, United States
View Trial DetailsNCT Number: NCT02752789
This is a multi-center, prospective, single cohort, observational study of pediatric heart transplant recipients designed to determine the impact of preformed versus de novo human leukocyte antigen (HLA) donor-specific antibodies (DSA), and antibodies to the self-antigens cardiac myosin and vimentin, on chronic allograft function. In addition, the investigators will explore mechanisms of action and predictors of DSA, rejection and altered pathophysiology.
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Notify MeUp to 20 year
All sexes
Observational
Hospital for Sick Children, Toronto, Canada
Participants that were enrolled in the CTOTC-04 study (ClinicalTrials.gov Identifier NCT01005316) are invited to enroll in this CTOTC-09 study. Conversion from the CTOTC-04 to CTOTC-09 study will occur in such a manner as to avoid/minimize discontinuity of follow-up between the planned CTOTC-04 and CTOTC-09 study visits. In addition, subjects added to the United Network for Organ Sharing (UNOS) system-or Canadian equivalent agency-at a participating study site, who are less than 21 years of age and fulfill all study eligibility criteria, will be invited to enroll in CTOTC-09.
This study focuses on the importance of antibodies against the newly transplanted heart in pediatric heart transplant recipients. The investigators aim to determine if certain antibodies lead to problems with the heart transplant. Antibodies are small proteins in the blood that the body makes to fight off infections, for example with bacteria or viruses. Since a new heart is "foreign" to the recipient's body, their immune system might try to attack it with antibodies, as if it were an infection. For many years it was thought that only white blood cells attacked the new heart, causing rejection.
Now there is new information showing that antibodies may also cause rejection or long-term damage to the heart. At this time, very little is known about how antibodies might cause problems after heart transplantation in transplant recipients younger than 21 years at the time of transplant.
This study will collect a medical history and blood samples at specified times for research. The blood samples will be used to measure antibodies in the blood, and to perform special tests to see how these antibodies might damage the heart.
Participant follow-up is from the day of the heart transplant to year 5 post-transplant.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
AND either:
-Enrolled in the CTOTC-04 study and actively followed at one of the study sites
OR
-Listed at participating study sites, less than 21 years of age and not yet transplanted.
The inclusion criteria for enrollment of new study patients in the CTOTC-09 Protocol will be the same as the CTOTC-04 study (refer to ClinicalTrials.gov ID NCT01005316).
Exclusion criteria
Time frame: 3 years post-transplantation
Time frame: 3 and 5 years post-transplantation
Cardiac hemodynamic findings: right and left ventricular end diastolic pressures, right atrial pressure, pulmonary artery pressure and cardiac index
Time frame: 3 years post-transplantation
Time frame: 3 years post-transplantation
Time frame: From >1 year to 5 years post-transplantation
Time frame: From >1 year to 5 years post-transplantation
Late acute rejection is defined as occurring >1 year post-transplantation
Time frame: Up to 5 years post-transplantation
Time frame: Up to 5 years post-transplantation
Recurrent defined as two or more late acute rejection episodes
Time frame: Up to 5 years post-transplantation
Time frame: Up to 5 years post-transplantation
Time frame: One year and up to 5 years post-transplantation
Time frame: 3 and 5 years post-transplantation
Time frame: 3 and 5 years
Graft function as assessed by echocardiography
Time frame: 3 and 5 years post-transplantation
Time frame: Up to 5 years post-transplantation
Time frame: Up to 5 years post-transplantation
Time frame: Up to 5 years post-transplantation
Time frame: Up to 5 years post-transplantation
Microvascular pathology as defined by:
Time frame: After exposure to alloantibody (or control) (At Year 1)
Endothelial Cell (EC) Culture Model is used to study factors that will predict and contribute to the protection of the graft following transplantation across sub-threshold concentrations of DSA. Exploratory: Expression of cytoprotective genes Bcl2 and HO-1, Intercellular adhesion molecules (ICAM), Vascular Cell Adhesion Molecule (VCAM) and selectins, Complement inhibitory proteins (cluster of differentiation antigen 55 (CD55), cluster of differentiation antigen 59 (CD59), Complement Receptor 1 (CR1), (CR2) and (CR3).
Time frame: 24 hours prior transplantation, Months 3 and 6 post transplantation
Cellular immune responses to allo-antigens and self-antigens (vimentin and myosin) will be measured by:
Time frame: Month 5 post transplantation
Role of IL-33 and its Receptor (ST2) in cardioprotection against effects of DSA will be measured by:
National Institute of Allergy and Infectious Diseases (NIAID)
Nih
An Observational Cohort Study to Determine the Impact of Alloantibodies and Antibodies to Self Antigens on Chronic Graft Function up to 5 Years After Pediatric Heart Transplantation (CTOTC-09)
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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