20
Participants
Start Date
April 1, 2017
Primary Completion Date
August 1, 2018
Study Completion Date
August 1, 2018
low-dose cosyntropin stimulation test
Each subject recruited in the study will undergo low dose cosyntropin stimulation test via intravenous short 2.5 cm plastic tube. 1 μg/ml ACTH aliquot stock solution will be pushed through, followed by 5 ml physiologic saline (0.9%). For each subject, serum and salivary cortisol will be measured just before cosyntropin administration and 30 minutes later.
Mira Koch, Haifa
Lead Sponsor
Bnai Zion Medical Center
OTHER_GOV