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Recruiting

NCT Number: NCT06387446

Allogeneic Valve Transplantation

Valves will be taken from hearts donated by organ donors, and implanted into patients who need a new heart valve.

Recruiting

Interested in participating?

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Key information

Age range

30 day–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Boston Children's Hospital

Boston, Massachusetts, 02115, United States

Location status: Recruiting

Location contact

Sitaram Emani, MD

CONTACT

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients requiring aortic, pulmonary, mitral or tricuspid valve replacement.
  • Pediatric patients 30 days or older and < 18 years, and adult patients 18-50 yrs.

o Particularly patients with significant growth potential

  • Insufficient options are available for valve replacement

o Patients at risk of immunogenic bio-prosthetic valve failure

  • Discussion with patient /family - option for durable valve rather than traditional prosthesis
  • ABO compatible
  • Patient and family able to travel to BCH within 48 hour time frame or within our organ procurement organization
  • Patients that are able to maintain follow-up at BCH during the duration of the study
  • Patients that are able to provide medical record authorization for 5 year follow-up

Exclusion criteria

  • Age < 30 days
  • Irreversible multisystem organ failure; or additive effects of the multiple systems affected making transplant survival unlikely
  • Progressive systemic disease with early mortality (genetic/metabolic, idiopathic, syndromic)
  • Morbid obesity (BMI>35)
  • Diabetes mellitus with evidence of end-organ damage
  • Severe chromosomal, neurologic or syndromic abnormalities
  • Immunocompromised condition (DiGeorge, SCID etc.)
  • Active infection
  • History of endocarditis
  • HIV or chronic hepatitis B or C infection
  • Malignancy within 5 years prior to transplant
  • Severe renal or liver failure
  • Inadequate social support for post-transplant management
  • Recent history of illicit drug, tobacco or alcohol abuse despite trials/assistance to stop behavior
  • Evidence of large stroke with high risk for hemorrhagic conversion
  • Heart transplant recipient
  • Patients that are unable to follow-up during the initial 6 month window
  • Patients that are unable to provide medical record authorization for 5 years

Treatment and study plan

Valve transplant

Procedure

Heart valves from an organ donor will be transplanted into recipient

Primary outcomes

  1. Valve Regurgitation

    Time frame: One year

    Heart valve regurgitation by echocardiogram. The degree of regurgitation is read and quantified by an echocardiologist.

  2. Valve Annulus Growth

    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.

  3. Leaflet Growth

    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.

Secondary outcomes

  1. Ventricular Function

    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.

  2. Survival

    Time frame: 5 years

    The number of patients that survive the initial procedure and long term outcomes.

Study contacts

Contact information is provided by the study sponsor or research team.

Sitaram Emani, MD

CONTACT

[email protected]

6173557899

Sponsors and collaborators

Lead sponsor

Boston Children's Hospital

Other

Registry information

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Apr 29, 2024
Registry last updated
Sep 24, 2024

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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