Clinical Trials Directory

Trials / Completed

CompletedNCT02621736

Copeptin for Prediction of Treatment Response in Children With Monosymptomatic Nocturnal Enuresis (MEN).

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

Summary

Monosymptomatic nocturnal enuresis (MEN) is a common problem in children, affecting 7-10% of all 7 year olds. MEN is often leading to psychosocial problems because of its burden and stigmatism. The only available medical treatment option is the vasopressin analogum Desmopressin®. However, according to the literature, only one third of patients shows a good treatment response, defined as more than 90% of reduced bed wetting. Furthermore, treatment with Desmopressin® may lead to psychosocial problems, high costs and potentially dangerous side effects like water intoxication and hypertension. Copeptin, mirroring arginine vasopressin (AVP), has been shown to be significantly lower in patients with MEN compared to controls and lower in patients with severe bed wetting compared to patients with only slight bed wetting.

Conditions

Interventions

TypeNameDescription
OTHERblood samplingAt 4 visits capillary blood sampling for copeptin measurement will be performed with each child.

Timeline

Start date
2016-01-01
Primary completion
2021-06-30
Completion
2021-06-30
First posted
2015-12-03
Last updated
2021-12-13

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT02621736. Inclusion in this directory is not an endorsement.