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Clinical Trial Summary

The are 2 principal goals in this study:

1. To measure plasma copeptin levels in healthy subjects and to correlate them with plasma AVP concentrations and urine osmolalities in iso-, hypo-, and hyperosmolar states.

2. To measure plasma copeptin concentrations in patients with chronic renal failure under the same conditions described above, in order to characterize the impact of renal function on circulating copeptin levels in correlation to plasma AVP and urine osmolality.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00696605
Study type Observational
Source Hospital Centre Biel/Bienne
Contact
Status Completed
Phase N/A
Start date July 2008
Completion date October 2009

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