Trials / Active Not Recruiting
Active Not RecruitingNCT07028645
Uroflowmetry and Nocturnal Enuresis
Is Uroflowmetry Useful in Assessing Response to Pharmacological Treatment in Enuresis
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (estimated)
- Sponsor
- Furkan Adem Canbaz · Academic / Other
- Sex
- All
- Age
- 5 Years – 17 Years
- Healthy volunteers
- Not accepted
Summary
This study will evaluate the uroflowmetry parameters of patients which were treated for enuresis.
Detailed description
A total of approximately 100 patients with enuresis will be evaluated retrospectively. Uroflowmetry parameters of these patients will be evaluated. For this purpose, patients will be divided to mainly three groups according to the treatment choices.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | desmopressin melt form 120 μg | Desmopressin 120 mcg will be used frist-line drug in the treatment of enuresis. |
| DRUG | Desmopressin lyophilisate (Melt) | Desmopressin 240 mcg will be used for the patients who have not responsive to desmopressin 120 mcg. |
| DRUG | Propiverine tablet | Propiverine (a dose of 0.8 mg/ kg) will be used for the patients who have -response to treatment with desmopressin 240 mcg |
Timeline
- Start date
- 2022-08-20
- Primary completion
- 2024-09-01
- Completion
- 2025-12-30
- First posted
- 2025-06-19
- Last updated
- 2025-06-24
Locations
1 site across 1 country: Turkey (Türkiye)
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07028645. Inclusion in this directory is not an endorsement.