Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
18 participants
OBSERVATIONAL
2015-11-30
2016-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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PROSPECTIVE
Study Groups
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observational
Blood samples will be taken for measuring copeptin levels in healthy subjects.
observation
blood sampling during 24 hours
Interventions
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observation
blood sampling during 24 hours
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* chronic illness
* pregnancy
* Anemia defined as Hb \< 30g/l
18 Years
50 Years
ALL
Yes
Sponsors
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University Hospital, Basel, Switzerland
OTHER
Responsible Party
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Principal Investigators
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Mirjam Christ-Crain, MD, Prof.
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Basel, Switzerland
Locations
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University Hospital Basel
Basel, Canton of Basel-City, Switzerland
Countries
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Other Identifiers
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EKNZ 2015-266
Identifier Type: -
Identifier Source: org_study_id
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