Clinical Trials Directory

Trials / Completed

CompletedNCT00238030

Thyroxine Replacement in Organ Donors

Efficacy and Pharmacokinetics of Oral Thyroid Replacement Therapy in Organ Donors

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
34 (actual)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Accepted

Summary

To compare oral versus intravenous administration of thyroid hormone: 1) for reversibility of hemodynamic instability in organ donors, and, 2) the pharmacokinetics of oral vs iv thyroid administration

Detailed description

Disruption of the hypothalamic-pituitary axis following brain death may lead to hemodynamic instability, peripheral vasodilation, and diabetes insipidus in organ donors, requiring the use of high doses of inotropes. Inotropes may cause ischemic injury to organs and intramyocardial ATP stores, resulting in organs unsuitable for transplantation, as well as, a reduction in post-transplant organ function. Therefore, some clinicians advocate the use of triple hormonal therapy in potential organ donors. Since intravenous T3(the intracellular active form of thyroxine) is unavailable, oral or intravenous T4 must be used, requiring the conversion of T4 to T3at the cellular level. This conversion is impeded by glucocorticoids which also are administered to organ donors for their immunomodulating effects. Since oral T3 is readily available, our first question is whether oral versus intravenous administration of T4 is comparable. If so, our next study is to determine the efficacy of oral T3 versus oral T4. Our hypothesis is oral T3 is superior to oral T4. Our study therefore will determine whether or not the oral route is suitable for administration of thyroid replacement therapy. The study will compare the pharmacokinetics of oral versus intravenous T4 administration in organ donors, as well as, determine its ability to wean intropes in this patient population.

Conditions

Interventions

TypeNameDescription
DRUGL-thryoxine2 mcg/kg iv or 2 mcg/kg po at time of enrollment
DRUGiv thryoxinethyroxine 2 mcg/kg iv

Timeline

Start date
2004-12-01
Primary completion
2009-05-01
Completion
2010-10-01
First posted
2005-10-13
Last updated
2011-01-05

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00238030. Inclusion in this directory is not an endorsement.