|
Main
|
|
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
|
Register:
|
ClinicalTrials.gov |
|
Last refreshed on:
|
12 December 2020 |
|
Main ID: |
NCT03074123 |
|
Date of registration:
|
03/03/2017 |
|
Prospective Registration:
|
Yes |
|
Primary sponsor: |
|
|
Public title:
|
Cortisol Response to Low Dose Cosyntropin Stimulation Test in the Late Afternoon
|
|
Scientific title:
|
Cortisol Response to Low Dose Cosyntropin Stimulation Test in the Late Afternoon |
|
Date of first enrolment:
|
April 1, 2017 |
|
Target sample size:
|
20 |
|
Recruitment status: |
Completed |
|
URL:
|
https://clinicaltrials.gov/show/NCT03074123 |
|
Study type:
|
Interventional |
|
Study design:
|
Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Diagnostic. Masking: None (Open Label).
|
|
Phase:
|
N/A
|
|
|
Countries of recruitment
|
|
Israel
| | | | | | | |
|
Contacts
|
|
Name:
|
Leonard Saiegh |
|
Address:
|
|
|
Telephone:
|
|
|
Email:
|
|
|
Affiliation:
|
Bni-Zion medical center |
| | |
|
Key inclusion & exclusion criteria
|
Inclusion Criteria:
healthy volunteers
Exclusion Criteria:
Clinical suspicion of hypoadrenalism Medical condition or treatment that might alter blood
cortisol levels Pregnancy
Age minimum:
18 Years
Age maximum:
70 Years
Gender:
All
|
|
Health Condition(s) or Problem(s) studied
|
|
Adrenal Insufficiency
|
|
Intervention(s)
|
|
Diagnostic Test: low-dose cosyntropin stimulation test
|
|
Primary Outcome(s)
|
|
Blood cortisol
[Time Frame: one day]
|
|
Secondary Outcome(s)
|
|
Salivary free cortisol
[Time Frame: one day]
|
|
Secondary ID(s)
|
|
0003-17BNZ
|
|
Source(s) of Monetary Support
|
|
Please refer to primary and secondary sponsors
|
|
Results
|
|
Results available:
|
|
|
Date Posted:
|
|
|
Date Completed:
|
|
|
URL:
|
|
|
|