Vesicoureteral Reflux Clinical Trial
Official title:
Determination of Voiding Patterns of Children With Vesicoureteral Reflux
NCT number | NCT00186199 |
Other study ID # | 1790 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | June 2005 |
Est. completion date | February 2012 |
Verified date | September 2022 |
Source | Stanford University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
Determine if the pattern of voiding differs in children with vesicoureteral reflux (VUR) compared to those who do not have VUR.
Status | Completed |
Enrollment | 38 |
Est. completion date | February 2012 |
Est. primary completion date | February 2012 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 3 Years to 16 Years |
Eligibility | Inclusion Criteria: - Children with or without vesicoureteral reflux (history of VUR) - Toilet trained and can void on command Exclusion Criteria: - Any voiding disorder, musculoskeletal neurologic disorders, other congenital or acquired genitourinary problems, growth disorders, recent UTI |
Country | Name | City | State |
---|---|---|---|
United States | Lucile Packard Childrens Hospital | Stanford | California |
Lead Sponsor | Collaborator |
---|---|
Stanford University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Uroflow rate | Obtain pre and postoperative uroflow after VUR correction | 3 months | |
Secondary | PVR | Pre and postoperative measures | 3 months |
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