Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:22 AM
Ignite Modification Date:
2025-12-25 @ 1:22 AM
NCT ID:
NCT06472193
Eligibility Criteria:
Inclusion Criteria:
* children with neurogenic bladder dysfunction, as an alternative route for catheterization for those who are unable or unwilling to utilize the native route being sensate urethra.
* in cases where bladder neck closure or reconstruction is necessary to achieve continence.
* Patients with urethral valves, prune belly syndrome and bladder exstrophy, performed either as an isolated procedure enabling patients to perform clean intermittent catheterization (CIC) or in relation with concomitant bladder augmentation
Exclusion Criteria:
patients clinically unfit for surgery patients underwent previous traditional Mitroffanof procedure
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Healthy Volunteers:
False
Sex:
ALL
Maximum Age:
18 Years
Study:
NCT06472193
Study Brief:
Protocol Section:
NCT06472193