Clinical Trials in Italy / NCT06764498
Active, not recruiting
Observational
Retrospective Study to Evaluate the Effectiveness of the Approach to Enuresis in Our Center
NCT06764498 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Enuresis
Study summary
Retrospective study to evaluate the effectiveness of the approach to enuresis at IRCCS Azienda Ospedaliero-Universitaria of Bologna Policlinico di Sant'Orsola, Italy.
Eligibility
Inclusion Criteria:
* Patients of either sex under the age of 18 years at the time of the first outpatient visit;
* Patients clinically evaluated in the outpatient clinic during the period 01/05/2019- 31/05/2021 with a diagnosis of enuresis;
* Patients presenting at least two outpatient follow-ups;
* Informed consent signed by parent or legal guardian.
Exclusion Criteria:
* Patients older than 18 years of age;
* Patients who lack completed night and daily diaries;
* Patients with continuous incontinence;
* Patients with neurological disorders and/or signs of spinal occult dysraphism;
* Patients with a severe cognitive disorder.
Primary outcome measure(s)
- Daily urinary frequency — at baseline
increase (≥8 micturitions/day) or decrease (≤3 micturitions/day) - Maximum Voided Volume (MVV) — at baseline
volume of urine emitted in 24 hours, excluding first morning urine - Bladder capacity — at baseline
reduction (\<35% of expected bladder capacity) or increase (\> 150% of expected bladder capacity)
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| IRCCS Azienda Ospedaliero-Universitaria di Bologna | Bologna | Italy |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06764498 on ClinicalTrials.gov ↗ ← All trials in Italy