search
Back to results

Intravenous Thyroxine for Heart-Eligible Organ Donors

Primary Purpose

Brain Death, Heart Failure

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Thyroxine
Saline
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Death focused on measuring Organ donor

Eligibility Criteria

14 Years - 55 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Declared dead by neurologic criteria (brain dead)
  • Authorization for organ donation and research
  • On one or more vasopressors and/or inotropes

Exclusion Criteria:

  • 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)

Sites / Locations

  • Donor Network of Arizona
  • Lifesharing
  • Donor Alliance
  • OurLegacy
  • Iowa Donor Network
  • Midwest Transplant Network
  • Louisiana Organ Procurement Agency
  • Mid-America Transplant Services
  • Lifebanc
  • LifeShare of Oklahoma
  • Southwest Transplant Alliance
  • Texas Organ Sharing Alliance
  • DonorConnect
  • LifeCenter Northwest

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Thyroxine

Saline Placebo

Arm Description

Intravenous thyroxine infusion

Intravenous saline infusion

Outcomes

Primary Outcome Measures

Heart transplanted
Whether heart is transplanted into living recipient
Graft function
30-day graft survival of hearts transplanted from study donors

Secondary Outcome Measures

Time till off vasopressors
Time in hours from randomization to when weaned off vasopressors (except vasopressin)
Weaned off vasopressors
Weaned off vasopressors within twelve hours
Time to order echo
Time till hemodynamic stability permits ordering initial echocardiogram
Ejection fraction
Left ventricular ejection fraction measured on first echocardiography

Full Information

First Posted
May 27, 2020
Last Updated
December 8, 2022
Sponsor
Washington University School of Medicine
Collaborators
Mid-America Transplant
search

1. Study Identification

Unique Protocol Identification Number
NCT04415658
Brief Title
Intravenous Thyroxine for Heart-Eligible Organ Donors
Official Title
A Multicenter Randomized Placebo-Controlled Trial of Intravenous Thyroxine for Heart-Eligible Brain Dead Organ Donors
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
December 1, 2020 (Actual)
Primary Completion Date
November 6, 2022 (Actual)
Study Completion Date
December 6, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine
Collaborators
Mid-America Transplant

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Death, Heart Failure
Keywords
Organ donor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
840 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Thyroxine
Arm Type
Experimental
Arm Description
Intravenous thyroxine infusion
Arm Title
Saline Placebo
Arm Type
Placebo Comparator
Arm Description
Intravenous saline infusion
Intervention Type
Drug
Intervention Name(s)
Thyroxine
Intervention Description
Infusion prepared by mixing 500 μg of drug in 500-ml of normal saline (i.e. concentration of 1 μg/ml) and enclosing the bag in an opaque sleeve. Infusion started at 30 μg/hour (30 ml/hour) for twelve hours.
Intervention Type
Drug
Intervention Name(s)
Saline
Intervention Description
The placebo will be a 500-ml bag of normal saline (without active drug) also enclosed in an opaque sleeve. This infusion will also be started at 30 ml/hour for twelve hours.
Primary Outcome Measure Information:
Title
Heart transplanted
Description
Whether heart is transplanted into living recipient
Time Frame
One week
Title
Graft function
Description
30-day graft survival of hearts transplanted from study donors
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Time till off vasopressors
Description
Time in hours from randomization to when weaned off vasopressors (except vasopressin)
Time Frame
72 hours
Title
Weaned off vasopressors
Description
Weaned off vasopressors within twelve hours
Time Frame
12 hours
Title
Time to order echo
Description
Time till hemodynamic stability permits ordering initial echocardiogram
Time Frame
72 hours
Title
Ejection fraction
Description
Left ventricular ejection fraction measured on first echocardiography
Time Frame
72 hours
Other Pre-specified Outcome Measures:
Title
Total organs transplanted
Description
Total number of organs transplanted
Time Frame
One week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Declared dead by neurologic criteria (brain dead) Authorization for organ donation and research On one or more vasopressors and/or inotropes Exclusion Criteria: 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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rajat Dhar, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Donor Network of Arizona
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85013
Country
United States
Facility Name
Lifesharing
City
San Diego
State/Province
California
ZIP/Postal Code
92108
Country
United States
Facility Name
Donor Alliance
City
Denver
State/Province
Colorado
ZIP/Postal Code
80230
Country
United States
Facility Name
OurLegacy
City
Maitland
State/Province
Florida
ZIP/Postal Code
32751
Country
United States
Facility Name
Iowa Donor Network
City
North Liberty
State/Province
Iowa
ZIP/Postal Code
52317
Country
United States
Facility Name
Midwest Transplant Network
City
Westwood
State/Province
Kansas
ZIP/Postal Code
66205
Country
United States
Facility Name
Louisiana Organ Procurement Agency
City
Covington
State/Province
Louisiana
ZIP/Postal Code
70433
Country
United States
Facility Name
Mid-America Transplant Services
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
Lifebanc
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44128
Country
United States
Facility Name
LifeShare of Oklahoma
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73132
Country
United States
Facility Name
Southwest Transplant Alliance
City
Dallas
State/Province
Texas
ZIP/Postal Code
75231
Country
United States
Facility Name
Texas Organ Sharing Alliance
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
DonorConnect
City
Murray
State/Province
Utah
ZIP/Postal Code
84107
Country
United States
Facility Name
LifeCenter Northwest
City
Bellevue
State/Province
Washington
ZIP/Postal Code
98006
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
30689222
Citation
Dhar R, Stahlschmidt E, Yan Y, Marklin G. A randomized trial comparing triiodothyronine (T3) with thyroxine (T4) for hemodynamically unstable brain-dead organ donors. Clin Transplant. 2019 Mar;33(3):e13486. doi: 10.1111/ctr.13486. Epub 2019 Feb 12.
Results Reference
background
PubMed Identifier
31802716
Citation
Dhar R, Stahlschmidt E, Marklin G. A Randomized Trial of Intravenous Thyroxine for Brain-Dead Organ Donors With Impaired Cardiac Function. Prog Transplant. 2020 Mar;30(1):48-55. doi: 10.1177/1526924819893295. Epub 2019 Dec 5.
Results Reference
background
PubMed Identifier
34838132
Citation
Dhar R, Klinkenberg D, Marklin G. A multicenter randomized placebo-controlled trial of intravenous thyroxine for heart-eligible brain-dead organ donors. Trials. 2021 Nov 27;22(1):852. doi: 10.1186/s13063-021-05797-2.
Results Reference
derived

Learn more about this trial

Intravenous Thyroxine for Heart-Eligible Organ Donors

We'll reach out to this number within 24 hrs