Trials / Unknown
UnknownNCT06301802
Outcomes of Proactive Management of Children With Myelomeningocele
Urological Outcomes of Proactive Management of Children With Myelomeningocele
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 40 (estimated)
- Sponsor
- Assiut University · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Accepted
Summary
Spina bifida birth prevalence in Africa is 0.13%. Myelomeningocele (MMC) represents the most frequent and most severe cause of NB in children. Treatment of neuropathic bladder secondary to spina bifida is an ongoing challenge. Damage of the renal parenchyma in children with NB is preventable given adequate evaluation, follow-up and proactive management. Proactive management was defined as use of clean intermittent catheterization (CIC), and/or anticholinergics at presentation, or based on initial high-risk urodynamic findings by 1 year of age. The proactive approach to treat SB (CIC and pharmacotherapy) has contributed to decreasing chronic kidney disease (CKD). Myelomeningocele is considered a complex congenital disease. Hence, a multidisciplinary team is the best choice for management of spina bifida, involving neurosurgeons, orthopedic surgeons, urologists, physical medicine and rehabilitation specialists and pediatricians. Currently, children with spina bifida in Egypt must visit multiple different locations to access the complex care they need. Here, we review our experience with patients with spina bifida who will be followed with this team with an emphasis on patients' upper urinary tract protection and decreasing urinary incontinence.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | CIC | clean intermittent catheterization |
| DRUG | Anticholinergic | antimuscarinic once daily |
Timeline
- Start date
- 2024-03-04
- Primary completion
- 2026-03-10
- Completion
- 2026-03-15
- First posted
- 2024-03-08
- Last updated
- 2024-03-08
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT06301802. Inclusion in this directory is not an endorsement.