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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01866137
Other study ID # PsyCo
Secondary ID
Status Completed
Phase N/A
First received May 13, 2013
Last updated September 8, 2014
Start date March 2013
Est. completion date February 2014

Study information

Verified date September 2014
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Observational

Clinical Trial Summary

The aim of the PsyCo Study is to determine whether psychological Stress has an influence on copeptin levels.


Description:

healthy volunteers undergo the TSST and stress hormones as cortisol and copeptin are measured


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date February 2014
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

•Aged over 18 years

Exclusion Criteria:

- Intake of any kind of medication (except birth control pill)

- BMI >30 kg/m2

- Evidence of any acute illness

- History of chronic illness

- Baseline glucose level >7 mmol/l Baseline sodium level <135 mmol/l or >145 mmol/l

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


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 Changes in copeptin levels after a psychological stress test in healthy volunteers 30min before, at time point 0, +10, +20, +40, +60 after the psychological stress test No
Secondary Changes in copeptin levels after a psychological stress test in patients with central diabetes insipidus Timpepoint 0, +10, +20, +40, +60 after the psychological stress test No
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