Unilateral Cutaneous Ureterostomy - Long Term Follow up (ureterostomy)

Sheba Medical Center

Status: Unknown

Conditions: Bladder Function

Study type: Observational

Funder types: Other

Identifiers

NCT00546208

SHEBA-07-4838-DZ-CTIL

Details and patient eligibility

About

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

Enrollment: 30 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

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)

Trial design

30 participants in 1 patient group

1

Description:

adolescents and young adults who underwent, as newborns, unilateral low loop cutaneous ureterostomy for severe bilateral hydro-ureteronephrosis, and that, afterwards, underwent stomal closure