Role of Intraoperative Thymoglobulin in Decreasing Ischemia-Reperfusion Injury in Pediatric Heart Transplant Recipients
Primary Purpose
Ischemia Reperfusion Injury, Heart Transplantation
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Anti-Thymocyte Globulin
Normal Saline
Sponsored by
About this trial
This is an interventional prevention trial for Ischemia Reperfusion Injury focused on measuring Ischemia Reperfusion Injury, Pediatric Heart Transplant, ATG, Induction Therapy
Eligibility Criteria
Inclusion Criteria:
- Pediatric population (ages 0-21 years)
- End-stage cardiac disease requiring heart transplantation
- Approval for listing by the UCLA Heart Transplant Committee
Exclusion Criteria:
- Prior documented Thymoglobulin allergy/adverse reaction
- History of or current diagnosis of lymphoma
- Documented lymphopenia
- Documented Thrombocytopenia
- Pregnancy
Sites / Locations
- Mattel Children's Hospital at UCLA
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
1
2
Arm Description
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00709293
First Posted
July 1, 2008
Last Updated
June 17, 2013
Sponsor
University of California, Los Angeles
Collaborators
Genzyme, a Sanofi Company
1. Study Identification
Unique Protocol Identification Number
NCT00709293
Brief Title
Role of Intraoperative Thymoglobulin in Decreasing Ischemia-Reperfusion Injury in Pediatric Heart Transplant Recipients
Official Title
Role of Intraoperative Thymoglobulin in Decreasing Ischemia-Reperfusion Injury in Pediatric Heart Transplant Recipients
Study Type
Interventional
2. Study Status
Record Verification Date
June 2013
Overall Recruitment Status
Withdrawn
Why Stopped
Insufficient funding
Study Start Date
July 2008 (undefined)
Primary Completion Date
May 2009 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
Genzyme, a Sanofi Company
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The restoration of normal blood flow following a period of ischemia may result in ischemia / reperfusion injury (I/RI), which is characterized by inflammation and oxidative damage to tissues. Varying degrees of I/RI occur upon reperfusion of a donor heart after cold storage. Medications containing antibodies against immune cells have been used for many years as powerful immunosuppressants. These medications, called polyclonal antibody preparations, are generally only used immediately following transplantation and/or to treat rejection. At our institution, one such antibody preparation (Thymoglobulin) is used in most pediatric heart transplant recipients for 3-5 days immediately after transplantation. Because standard immunosuppressive medications (called calcineurin inhibitors) are toxic to the kidneys, the use of Thymoglobulin allows us to delay the initiation of calcineurin inhibitors until the kidneys of completely recovered from the shock of the transplant surgery.
We hypothesize that Thymoglobulin may be beneficial in reducing the damage caused by I/RI. Thus, the present study seeks to evaluate the effectiveness of an intra-operative dose of Thymoglobulin (in addition to the standard doses post-operatively) at reducing the effects of I/RI. The study will be a double-bind placebo-controlled trial involving 20 subjects. Biologic markers for I/RI will be assessed at periodic intervals for six months post-transplantation. Subjects receiving intra-operative doses of Thymoglobulin will be compared to the controls in order to assess the effectiveness of intra-operative Thymoglobulin in ameliorating the effects of I/RI.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemia Reperfusion Injury, Heart Transplantation
Keywords
Ischemia Reperfusion Injury, Pediatric Heart Transplant, ATG, Induction Therapy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Placebo Comparator
Arm Title
2
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Anti-Thymocyte Globulin
Other Intervention Name(s)
ATG
Intervention Description
Thymoglobulin (1.5 mg/kg body weight) will be infused through a peripheral intravenous line over a minimum of 6 hours. The infusion will be started at the time of donor visualization (once it is confirmed the transplant is proceeding). The peri-operative nurse or anesthesiologist will be responsible for drug infusion.
Intervention Type
Drug
Intervention Name(s)
Normal Saline
Intervention Description
Normal saline will be utilized as a placebo comparator. It will be infused in the same fashion as the Thymoglobulin in the intervention arm.
10. Eligibility
Sex
All
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pediatric population (ages 0-21 years)
End-stage cardiac disease requiring heart transplantation
Approval for listing by the UCLA Heart Transplant Committee
Exclusion Criteria:
Prior documented Thymoglobulin allergy/adverse reaction
History of or current diagnosis of lymphoma
Documented lymphopenia
Documented Thrombocytopenia
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan C Alejos, MD
Organizational Affiliation
Department of Pediatrics, University of California Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mattel Children's Hospital at UCLA
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Role of Intraoperative Thymoglobulin in Decreasing Ischemia-Reperfusion Injury in Pediatric Heart Transplant Recipients
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