EUCTR2015-004406-42-ES进行中（未招募）1 期
CLINICAL TRIAL TO ASSEES THE NON-INFERIORITY OF THE SUSPENSION OF PROPHYLACTIC TREATMENT WITH VALGANCICLOVIR IN KIDNEY TRANSPLANT CMV-seropositive PATIENTS, WHO MANTEIN CD8+ CMV- CELLULAR IMMUNITY AFTER THYMOGLOBULIN TREATMENT.
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- FIBICO
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •CMV-seropositive kidney transplant,
- •CD8 + T cell immunity specific pretransplant CMV (CMV-reactive
- •Quantiferon pretraspante)
- •> 18 years (adult)
- •Receiving induction therapy with Thymoglobulin
- •Receiving prophylaxis with valganciclovir.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 150
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •Multivisceral transplants including kidney-pancreas
- •HIV-infected patients
- •Patients who can not comply with the monitoring protocol
研究者
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