Clinical Trials Directory

Trials / Completed

CompletedNCT01940614

Use of Copeptin in Diabetes Insipidus

Use of Copeptin in the Differential Diagnosis of Diabetes insipidus-a Prospective International Study

Status
Completed
Phase
Study type
Observational
Enrollment
156 (actual)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
16 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Prospective evaluation of the novel biomarker copeptin in the differential diagnosis of diabetes insipidus against the standard diagnostic test methods.

Detailed description

Purpose of this study is to compare the overall diagnostic accuracy of the three following diagnostic test procedures in diabetes insipidus (central, nephrogenic) and primary polydipsia: a) classical water deprivation test alone, b) classical water deprivation test plus plasma copeptin cut-off levels, c) hypertonic saline infusion test plus plasma copeptin measurement. The investigators hypothesize that firstly b) and c) is better as a). Secondly the investigators hypothesize that c) is non-inferior to b).

Conditions

Interventions

TypeNameDescription
OTHERWater deprivation testClassical water deprivation test alone
OTHERWater deprivation testclassical water deprivation test plus plasma copeptin cut-off levels
OTHERHypertonic saline infusionhypertonic saline infusion test plus plasma copeptin measurement

Timeline

Start date
2013-07-01
Primary completion
2017-06-01
Completion
2017-12-01
First posted
2013-09-12
Last updated
2018-04-17

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT01940614. Inclusion in this directory is not an endorsement.