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Daclizumab Experience in Pediatric Heart Transplant

C

Children's Healthcare of Atlanta

Status

Terminated

Conditions

Congenital Disorders

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to examine the outcomes of those who have received Daclizumab as part of their immuno-suppression protocol following heart transplantation. Literature suggests that the time to first rejection episode can be avoided or delayed by using induction therapy.

Full description

In August 2005 the heart transplant team at Children's Healthcare of Atlanta began a protocol of Daclizumab 1mg/kg IV every two weeks for 5 doses; 1st dose to be received in the operating room following discontinuation of cardiopulmonary bypass.

Since one year has passed following initiation of this practice, it is necessary to review this immuno-suppression strategy and determine if, in fact, there was clinical benefit of reducing rejection without increasing the vulnerabilities of the immuno-compromised host.

We wish to review all heart transplant recipient records between August 1, 2004 and October 15, 2006. Historically, Children's has done approximately 10 transplants per year; therefore, we will review approximately 15 charts at Children's Healthcare of Atlanta and Sibley Heart Center Cardiology.

Enrollment

30 patients

Sex

All

Ages

Under 21 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Status post heart transplant
  • Age 0-21 years
  • Received Daclizumab as induction therapy

Exclusion criteria

  • Those who do not meet inclusion criteria

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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