Boston Children's Hospital
Boston, Massachusetts, 02115, United States
Location status: Recruiting
Location contact
Sitaram Emani, MD
CONTACT
NCT Number: NCT06387446
Valves will be taken from hearts donated by organ donors, and implanted into patients who need a new heart valve.
Interested in participating?
Request Info30 day–50 year
All sexes
Interventional
Not applicable
Boston, Massachusetts, 02115, United States
Location status: Recruiting
Sitaram Emani, MD
CONTACT
Heart valves in children and young adults may need replacement or repair. In many children the options for heart valve replacement do not grow as the child grows. A transplanted valve may have the option to grow with time and may reduce the need for multiple operations over a lifetime. This trial will study the outcomes of heartfelt transplant in children and young adults undergoing this procedure. The study will look at outcomes of valve transplant and any potential side effects.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
o Particularly patients with significant growth potential
o Patients at risk of immunogenic bio-prosthetic valve failure
Exclusion criteria
Heart valves from an organ donor will be transplanted into recipient
Time frame: One year
Heart valve regurgitation by echocardiogram. The degree of regurgitation is read and quantified by an echocardiologist.
Time frame: One Year
Measurement of valve annulus via echocardiogram, CT scan and MRI. This will be quantified by whether or not the annulus continues to increase in size as the subject grows.
Time frame: One Year
Measurement of leaflet height via echocardiogram, CT scan and MRI and reviewed by an echocardiologist. This will be analyzed by whether or not the leaflets continue to grow in size, with the subject.
Time frame: One year
Ventricular function will be visualized using echocardiogram, measured as ejection fraction as well as shortening fraction and will be determined by an echocardiologist. The factors involved will be the symmetrical squeeze of the ventricles, the ejection fraction, ventricular end systolic and diastolic volume with calculation of stroke volume to come to a surrogate of cardiac output.
Time frame: 5 years
The number of patients that survive the initial procedure and long term outcomes.
Contact information is provided by the study sponsor or research team.
Boston Children's Hospital
Other
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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