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Clinical Trial Summary

The aim of this study is to investigate whether oral urea stimulates copeptin release and, if so, whether it may provide a novel diagnostic test in the differentiation between AVP-D (Arginine vasopressin deficiency) and PP (primary polydipsia).


Clinical Trial Description

This study consists of two parts, including healthy adults (study part 1 - proof of concept) and adults with an established diagnosis of PP or AVP-D (study part 2 - pilot study). If the results of study part 1 suggest that oral urea is a potent stimulator of copeptin in healthy adults, study part 2 will be conducted, meaning that adults with an established diagnosis of PP or AVP-D will be included. If study part 1 demonstrates no relevant copeptin increase in response to oral urea, the study will be terminated thereafter and study part 2 will not be conducted. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05890690
Study type Interventional
Source University Hospital, Basel, Switzerland
Contact Mirjam Christ-Crain, Prof.
Phone +41 61 328 70 80
Email mirjam.christ-crain@usb.ch
Status Recruiting
Phase N/A
Start date June 2, 2023
Completion date December 2024

See also
  Status Clinical Trial Phase
Completed NCT02770885 - Effects of GLP-1 Analogues on Fluid Intake in Patients With Primary Polydipsia (The GOLD-Study) Phase 2
Completed NCT01940614 - Use of Copeptin in Diabetes Insipidus