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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date September 2022
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Determine if the pattern of voiding differs in children with vesicoureteral reflux (VUR) compared to those who do not have VUR.


Description:

We hope to determine the statistical difference between the flow rate and volume of urination in children with VUR compared to those without.


Recruitment information / eligibility

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

Study Design


Locations

Country Name City State
United States Lucile Packard Childrens Hospital Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

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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