The primary objective of this study is to evaluate the feasibility of a randomized controlled trial comparing levothyroxine to placebo in neurologically deceased donors
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Enrollment
15
20 mg IV bolus + 10 mg/h infusion
Hopital du Sacré-Coeur de Montreal
Montreal, Quebec, Canada
Study feasibility
1\) proportion of eligible recruited patients 2)proportion of recruited patients who completed the study 3) proportion of protocol violation
Time frame: In 2 years
Variation in left ventricular ejection fraction
Time frame: 6 hours post infusion
Numbers of donated hearts
Time frame: On organ donation surgery
Incidence of de novo atrial fibrillation
Time frame: From beginning of infusion until beginning of retrieval surgery
Time from recruitment to the administration of the study drug
Time frame: From randomization to 12 hours post randomization
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