Unilateral Cutaneous Ureterostomy - Long Term Follow up
- Conditions
- Bladder Function
- Registration Number
- NCT00546208
- Lead Sponsor
- Sheba Medical Center
- Brief Summary
This observational study is aimed at exploring bladder function following temporary unilateral low loop cutaneous ureterostomy carried out in newborns suffering from severe congenital hydro-ureteronephrosis
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Living patients
- Bilateral functioning kidneys
- Unilateral ureteral cutaneous diversion
Exclusion Criteria
- Dead patients
- Single kidney
- High percutaneous ureteral diversion (e.g: cutaneous pyelostomies, bilateral cutaneous urinary diversion)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
The Chaim Sheba Medical Center, Tel Hashomer
🇮🇱Ramat Gan, Israel