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临床试验/NCT04415658
NCT04415658已完成3 期

A Multicenter Randomized Placebo-Controlled Trial of Intravenous Thyroxine for Heart-Eligible Brain Dead Organ Donors

Washington University School of Medicine14 个研究点 分布在 1 个国家目标入组 838 人开始时间: 2020年12月1日最近更新:
适应症
干预措施
相关药物

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

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

Experimental

Intravenous thyroxine infusion

干预措施: Thyroxine (Drug)

Saline Placebo

Placebo Comparator

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

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

Rajat Dhar

Professor

Washington University School of Medicine

研究点 (14)

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Intravenous Thyroxine for Heart-Eligible Organ Donors | 临床试验