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临床试验/NCT00966836
NCT00966836Unknown3 期

Efficacy and Safety of Anti-cytomegalovirus Prophylaxis Versus Pre-emptive Approaches With Valganciclovir in Heart Transplant Recipients Treated With Everolimus or Mycophenolate. A Randomized Open-label Study for Prevention of Cardiaca Allograft Vasculopathy

University of Bologna1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2009年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
发起方
入组人数
100
试验地点
1
主要终点
Change in maximal intimal thickness

研究概览

简要总结

Cardiac allograft vasculopathy (CAV) is the major cause of long-term graft failure in heart transplant recipients. Although several immune-mediated and metabolic risk factors have been implicated in the pathogenesis of CAV, no effective therapy is currently available to treat established CAV and prevent its adverse outcomes. Therefore, the main clinical strategy is based on prevention and treatment of factors known to trigger its development. Although the mechanism is vague, cytomegalovirus (CMV) infection is believed to play a key role in CAV progression.

Two strategies involving administration of specific anti-CMV agents are recommended for prevention of CMV infection/disease: universal prophylaxis and preemptive therapy. The pros and cons of the two strategies are still debated, in the absence of randomized studies addressing graft-related outcomes and viral mechanisms of graft damage, and without any clear evidence of superiority of either approach.

The investigators conceived this randomized prospective project to compare the effect of preemptive anti-CMV strategy with universal anti-CMV prophylaxis on CMV infection and on one-year increase in coronary intimal thickening. Patients will be additionally randomized to receive either mycophenolate mofetil or everolimus, in light of the possible anti-CMV properties of everolimus.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18y
  • Heart or heart-kidney combined transplant
  • Positive CMV serology at the time of transplant
  • Glomerular filtration rate ≥ 20 ml/min/1.73m2 with MDRD at randomization.
  • Written informed consent

排除标准

  • Panel Reactive Antibody ≥50%
  • Less than 1000/mmc neutrophils at the time of randomization
  • Less than 30,000/mmc platelets at the time of randomization
  • Clinical significant infection in the 2 weeks prior to transplant
  • Glomerular filtration rate < 20 ml/min/1.73m2 estimated with MDRD formula at the time of randomization or hemodialysis treatment
  • Intolerance towards valganciclovir, everolimus, mycophenolate or cyc-losporine
  • Known contraindication to statin use
  • Negative CMV serology at the time of transplant
  • HIV positive testing
  • Severe comorbidities that, based on investigator's judgment, contraindicate study drugs or procedures
  • Potentially childbearing women who refuse to use contraceptives
  • Participation to an interventional study in the 2 preceding weeks
  • Unwillingness or inability to follow study procedure and to sign written in-formed consent

研究组 & 干预措施

Pre-emptive everolimus

Experimental

干预措施: Pre-emptive strategy with valganciclovir plus everolimus (Drug)

Prophylaxis mycophenolate

Experimental

干预措施: Prophylaxis with valganciclovir plus mycophenolate (Drug)

Prophylaxis Everolimus

Experimental

干预措施: Prophylaxis with valganciclovir plus everolimus (Drug)

Pre-emptive mycophenolate

Active Comparator

干预措施: Pre-emptive mycophenolate (Drug)

结局指标

主要结局

Change in maximal intimal thickness

时间窗: one year

次要结局

  • CMV infection(one year)

研究者

发起方
University of Bologna
申办方类型
Other

研究点 (1)

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