Circadian Rhythm Clinical Trial
— Co-RhythmOfficial title:
The Circadian Rhythm of Copeptin
Verified date | August 2016 |
Source | University Hospital, Basel, Switzerland |
Contact | n/a |
Is FDA regulated | No |
Health authority | Switzerland: Ethikkommission |
Study type | Observational |
The circadian rhythm of copeptin will be examined in healthy subjects.
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 |
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 | 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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