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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02604875
Other study ID # EKNZ 2015-266
Secondary ID
Status Completed
Phase N/A
First received November 10, 2015
Last updated August 12, 2016
Start date November 2015
Est. completion date April 2016

Study information

Verified date August 2016
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

The circadian rhythm of copeptin will be examined in healthy subjects.


Description:

In 18 healthy volunteers the circadian rhythm of copeptin will be examined by withdrawing blood samples for copeptin levels every 30 minutes for 24 hours.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- healthy subjects

Exclusion Criteria:

- acute illness

- chronic illness

- pregnancy

- Anemia defined as Hb < 30g/l

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
observation
blood sampling during 24 hours

Locations

Country Name City State
Switzerland University Hospital Basel Basel Basel-Stadt

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary measurement of copeptin values in mmol/l within 24 hours to assess the amount of release in a day curve. The primary outcome measure is to compare the copeptin concentration in the early afternoon and the early morning by blood sampling at different time points. Evaluation of the question if there is a circadian rhythm in the copeptin release. 24 hours No
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