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Sponsored by: |
Sheba Medical Center |
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Information provided by: | Sheba Medical Center |
ClinicalTrials.gov Identifier: | NCT00546208 |
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
Condition |
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Bladder Function |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | Bladder Function Following Temporary Unilateral Cutaneous Ureterostomy - Long Term Follow up |
Estimated Enrollment: | 30 |
Study Start Date: | February 2008 |
Groups/Cohorts |
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1
adolescents and young adults who underwent, as newborns, unilateral low loop cutaneous ureterostomy for severe bilateral hydro-ureteronephrosis, and that, afterwards, underwent stomal closure
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Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
adolescents and adults who had been operated in our institution for severe bilateral congenital hydro-ureteronephrosis
Inclusion Criteria:
Exclusion Criteria:
Contact: Dorit E Zilberman, MD | +97235302231 | dorit.zilberman@sheba.health.gov.il |
Israel | |
The Chaim Sheba Medical Center, Tel Hashomer | Recruiting |
Ramat Gan, Israel, 52621 | |
Contact: Dorit E Zilberman, MD +973-3-5302231 dorit.zilberman@sheba.health.gov.il | |
Sub-Investigator: Yoram Mor, MD |
Principal Investigator: | Dorit E Zilberman, MD | The Chaim Sheba Medical Center |
Responsible Party: | Urology Department, Chaim Sheba Medical Center ( Dorit Zilberman ) |
Study ID Numbers: | SHEBA-07-4838-DZ-CTIL |
Study First Received: | October 17, 2007 |
Last Updated: | March 13, 2008 |
ClinicalTrials.gov Identifier: | NCT00546208 History of Changes |
Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
bladder function cutaneous ureterostomy hydronephrosis |
Hydronephrosis |