Determination of Voiding Patterns of Children With Vesicoureteral Reflux

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

Completed

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Key information

Conditions

Vesicoureteral Reflux Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Male Urogenital Diseases Urinary Bladder Diseases Urogenital Diseases Urologic Diseases Vesico-Ureteral Reflux

Age range

3 year–16 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Lucile Packard Childrens Hospital

Stanford, California, 94305, United States

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

Uroflow rate

Time frame: 3 months

Obtain pre and postoperative uroflow after VUR correction

Secondary outcomes

PVR

Time frame: 3 months

Pre and postoperative measures

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Important dates

Study start: 2005
Primary completion: 2012
Study completion: 2012
First posted: Sep 16, 2005
Registry last updated: Sep 14, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed