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临床试验/NCT00166153
NCT00166153终止不适用

The Relationships Between Mycophenolic Acid Levels, T-Cell Subsets and Outcomes in Pediatric Heat Transplant Recipients Receiving Mycophenolate Mofetil (Cellcept)

Emory University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2003年1月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
30
试验地点
2
主要终点
Examine t-cell subsets to determine the correlation between MIP levels and clinical outcome as well as effect on T-cell proliferation.

研究概览

简要总结

The survival of children who have received heart transplants has greatly improved over the last ten years. One reason for this is better control over rejection. Rejection medications require a delicate balance of enough medicine to work without causing side effects. It is a goal to avoid both rejection and side effects from the anti-rejection medicines. Usually several medicines are used together to prevent rejection. One of these medicines is often Mycophenolic Acid or CellceptThis medicine has been used longer for adults than is has for children. More information is needed on using it for children. The dose is usually determined by the patient's weight or body surface area.

There have been some early studies of the use of Cellcept, but none have proven a relationship between the blood level of the drug and how well it works. More also needs to be known about how this drug works with other anti-rejection drugs and how it works in boys and girls. This study will look more closely at proper dosing, how Cellcept works with other anti-rejection medications, side effects, and any differences in how this medicine works in boys and girls.

All patients in the study will be receiving Cellcept and have blood levels of the drug drawn. Results of their usual treatment and testing will be recorded and evaluated for signs of rejection. All the information will be analyzed. Results of this study will be reported to transplant committees locally and nationally.

详细描述

Pediatric heart transplant recipients receiving MMF will undergo study testing to measure MPA levels by the HPLC method and T-cell subsets by flow cytometry method. As standard of care they receive histological grading of routine endomyocardial biopsies using the International Society of Heart Lung Transplantation (ISHLT) grading scale. The data obtained from standard assessments will include medications, echocardiographic reports, pre-and post biopsy assessments/physical exams, hospital records for any inpatient hospitalization, and any laboratory assessments. Also, information will be collected on all patients which will be examined for tolerance and success (side effects and rejection) of immunosuppressive therapy.

In newly transplanted patients, study testing will occur at the same time as standard of care biopsies which are typically 1 week, 2 weeks, 3 weeks, 4 weeks, 6 weeks, 8 weeks, 3 months, 4 months, 5 months, 6 months, 8 months, 10 months, 12 months. If the patient has additional visits due to rejection or changes in immunosuppression, then more frequent study testing may be done per investigator preference. Previously transplanted patients will have study testing at the same time as their standard of care visits, usually annually.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
2 Weeks 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Heart Transplant Recipients who are transplanted during the course of this study.
  • Age 2 weeks to 18 years
  • Receiving or plan to receive Mycophenolate mofetil therapy
  • Patient/Family has signed an informed assent/consent

排除标准

  • Patients that are unable to follow protocol schedule of assessment
  • Patients with chronic autoimmune disease
  • Patients who have received a multiple organ transplant (i.e. heart-liver, heart-lung etc.)

结局指标

主要结局

Examine t-cell subsets to determine the correlation between MIP levels and clinical outcome as well as effect on T-cell proliferation.

次要结局

  • Examine histologic grading of routine endomyocardial biopsies to determine the correlation between MPS levels and acute rejections.

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kirk R. Kanter, MD

Principal Investigator

Emory University

研究点 (2)

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