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
| Type | Name | Description |
|---|---|---|
| OTHER | blood sampling | At 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.