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临床试验/NCT00027443
NCT00027443已完成不适用

Giant Cell Myocarditis Treatment Trial Pilot Study

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2001年8月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
40
试验地点
1

研究概览

简要总结

This is a study to determine the efficacy of muromonab-CD3 and cyclosporine as treatment in patients with giant cell myocarditis (GCM). T lymphocytes appear to be involved in GCM. Muromonab-CD3 has been shown to reduce the number of lymphocytes and cyclosporine inhibits lymphocyte activation. This treatment may prolong patient survival until transplantation or ventricular assist device placement is possible.

详细描述

Each patient will be randomized to receive either standard care and immunosuppression therapy (treatment group) or standard care alone (control group). To prevent bias, randomization will be stratified by recency of symptom onset to ensure that both the treatment and control groups are balanced with respect to it. Within each of these 2 strata, permuted-block randomization will be done to keep the number of treatment and control patients balanced. Due to the necessary monitoring of the patients randomized to receive immunosuppression therapy, treatment cannot be blinded. Approximately 1 year after the last patient has been randomized, the observed times from randomization to the composite endpoint (death, transplantation, or LVD placement) will be compared in the treatment and control groups.

Completion date provided represents the completion date of the grant per OOPD records

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Idiopathic heart failure and/or arrhythmia of less than 3 months duration
  • •Endomyocardial biopsy diagnostic of idiopathic giant cell myocarditis
  • •Negative pregnancy test

排除标准

  • •Clinical evidence of sepsis or active infection (e.g., meningitis or osteomyelitis)
  • •Any contraindication to immunosuppression
  • •Allergy to cyclosporine or muromonab-CD3
  • •Creatinine greater than 2.5 mg/dL
  • •AST or ALT greater than 3 times upper limit of normal
  • •Other severe concurrent disease that would preclude study
  • •Unreliable or uncooperative subject

研究者

发起方
Mayo Clinic
申办方类型
Other

研究点 (1)

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