Stress Clinical Trial
— PsyCoOfficial title:
Copeptin During a Standardized Psychological Stress Test
Verified date | September 2014 |
Source | University Hospital, Basel, Switzerland |
Contact | n/a |
Is FDA regulated | No |
Health authority | Switzerland: Swissmedic |
Study type | Observational |
The aim of the PsyCo Study is to determine whether psychological Stress has an influence on copeptin levels.
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 |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Switzerland | University Hospital Basel | Basel | Basel-Stadt |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Basel, Switzerland |
Switzerland,
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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