A Multicenter Randomized Placebo-Controlled Trial of Intravenous Thyroxine for Heart-Eligible Brain Dead Organ Donors
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 838
- 试验地点
- 14
- 主要终点
- Graft Function
研究概览
简要总结
This randomized controlled trial will evaluate whether intravenous thyroxine infusion given to brain-dead organ donors who are eligible to donate hearts for 12 hours will result in more hearts transplanted than saline placebo
详细描述
Background: Brain death frequently induces hemodynamic instability and cardiac stunning. Impairments in cardiac performance are major contributors to hearts from otherwise eligible organ donors not being transplanted. Deficiencies in pituitary hormones (including thyroid stimulating hormone) may contribute to hemodynamic instability and replacement of thyroid hormone has been proposed as a means of improving stability and increasing hearts available for transplantation. Intravenous thyroxine is commonly used in donor management. However, small controlled trials have not been able to demonstrate efficacy.
Methods: This multicenter study will involve organ procurement organizations (OPOs) across the country. A total of 800 heart-eligible brain dead organ donors who require vasopressor support will be randomly assigned to intravenous thyroxine for at least 12-hours or saline placebo. The primary study hypothesis is that thyroxine treatment results in more hearts transplanted. Additional outcome measures are time to achieve hemodynamic stability (weaning off vasopressors) and improvement in cardiac ejection fraction on echocardiography.
Discussion: This will be the largest randomized controlled study to evaluate the efficacy of thyroid hormone treatment for organ donor management. By collaborating across multiple OPOs, it will be able to enroll an adequate number of donors and be powered to definitively answer the critical question of whether treatment increases hearts transplanted and/or provides other hemodynamic benefits.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 14 Years 至 55 Years(Child, Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Declared dead by neurologic criteria (brain dead)
- •Authorization for organ donation and research
- •On one or more vasopressors and/or inotropes
排除标准
- •Brain death declared more than 24 hours prior
- •Only vasopressor is vasopressin
- •Weight < 45 kg (100 lbs)
- •Known coronary artery disease or history of myocardial infarction
- •Known valvular heart disease
- •Prior sternotomy or cardiac surgery
- •Donor at VA hospital
- •Received intravenous or oral thyroxine within past month
- •Known HIV+ status
- •Other reason donor is unable to receive study drug (determined by on-site personnel)
研究组 & 干预措施
Thyroxine
Intravenous thyroxine infusion
干预措施: Thyroxine (Drug)
Saline Placebo
Intravenous saline infusion
干预措施: Saline (Drug)
结局指标
主要结局
Graft Function
时间窗: 30 days
30-day graft survival of hearts transplanted from study donors, obtained from SRTR recipient registry
Heart Transplanted
时间窗: One week
Whether heart is transplanted into living recipient
次要结局
- Time Till Off Vasopressors(72 hours)
- Weaned Off Vasopressors(12 hours)
- Ejection Fraction(72 hours)
- Time to Order Echo(72 hours)
- Lungs Transplanted(72 hours)
研究者
Rajat Dhar
Professor
Washington University School of Medicine
