Retrospective Study to Evaluate the Effectiveness of the Approach to Enuresis in Our Center (NCT06764498) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Retrospective Study to Evaluate the Effectiveness of the Approach to Enuresis in Our Center
Italy200 participantsStarted 2022-02-10
Plain-language summary
Retrospective study to evaluate the effectiveness of the approach to enuresis at IRCCS Azienda Ospedaliero-Universitaria of Bologna Policlinico di Sant'Orsola, Italy.
Who can participate
Age range
17 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Daily urinary frequency
Timeframe: at baseline
2
Maximum Voided Volume (MVV)
Timeframe: at baseline
3
Bladder capacity
Timeframe: at baseline
Trial details
NCT IDNCT06764498
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna