Enuresis. nonorganic enuresis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 6 to 12 years old Single-symptom nocturnal enuresis Able to use nasal spray or sublingual tablets Completion of the informed consent form by the guardian or legal guardian At least two weeks before the start of the study, he did not receive any medicine
Exclusion criteria
Exclusion criteria: Having a history of organic urological disease, daily urinary incontinence, diabetes insipidus, or persistent urinary tract infection Having clinically significant renal, hepatic, gastrointestinal, pulmonary, cardiovascular, endocrine, or neurological disease that interferes with evaluation Using antibiotics, diuretics or any medicine that affects the concentration of urine Failure to complete the informed consent form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nocturia frequency. Timepoint: The period before the study, during one month after starting the drug and the follow-up period three months later. Method of measurement: Recording wet or dry nights in a notebook, by parents. | — |
Countries
Iran (Islamic Republic of)
Contacts
Mashhad University of Medical Sciences