Current partner codePEPTIDESDE
NCT07028645·Not applicable·OBSERVATIONAL

Uroflowmetry and Nocturnal Enuresis

Status

Active, not recruiting

Phase

Not applicable

Enrollment

100

Locations

1

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

This study will evaluate the uroflowmetry parameters of patients which were treated for enuresis.

Full 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.

Interventions

Treatment arms and agents.

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

From registration to results.

  1. First posted

    Jun 19, 2025

  2. Study start

    Aug 20, 2022

  3. Primary completion

    Sep 1, 2024

  4. Study completion

    Dec 30, 2025

  5. Results posted

    Not reported

  6. Registry updated

    Jun 24, 2025

Outcomes

What the study measures.

Primary outcomes

Number of days without bedwetting

Time frame · 1 month

Achievement of bedwetting in one or less night of a month

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
5 Years
Maximum age
17 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Presence of enuresis nocturna * Patients who have uroflowmetry test Exclusion Criteria: * Presence of lower urinary tract symptoms * Presence of anatomical or neurological problems * Patients with missing data

Study locations

1 registered sites.

Turkey (Türkiye). Showing up to 24 locations stored in the fast local snapshot.

Sancaktepe Sehit Prof dr Ilhan Varank Training and Research Hospital

Istanbul, Kadikoy, Turkey (Türkiye)

Related trials

More studies on Desmopressin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.