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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01056887
Other study ID # 17121979
Secondary ID 33/07
Status Completed
Phase N/A
First received January 25, 2010
Last updated April 22, 2011
Start date March 2008
Est. completion date November 2010

Study information

Verified date November 2010
Source University of Wuerzburg
Contact n/a
Is FDA regulated No
Health authority Germany: The Bavarian State Ministry of the Environment and Public Health
Study type Observational

Clinical Trial Summary

The differential diagnosis of patients with polyuria/ polydipsia is often complex, but important for the therapeutic strategy.

Challenging is in particular the clinical differentiation between patients with a partial Diabetes insipidus centralis and patients with primary polydipsia as underlying disease, because both groups are associated with similar urinary osmolalities.

The determination of plasma arginine vasopressin is unusual in this context, since measurement of AVP is not reliably.

C-terminal ProVasopressin (copeptin) is secreted stoichiometrically with AVP from the neurohypophysis, but has a longer half life in the circulation, and is thus easier to measure.

Therefore, the investigators will analyze in that study the diagnostic utility of plasma copeptin in the differential diagnosis of polyuria and polydipsia.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date November 2010
Est. primary completion date November 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients with polydipsia/ polyuria, with indication for performing a deprivation test

- > 18 years

Exclusion Criteria:

- dDAVP during the last 14d

- pregnancy

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Univ Hospital Wuerzburg Wuerzburg Bavaria

Sponsors (2)

Lead Sponsor Collaborator
University of Wuerzburg Dr. Carson Liu Med Corp.

Country where clinical trial is conducted

Germany, 

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