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Completed Phase 3 Interventional Results available

Randomized Intervention for Children With Vesicoureteral Reflux (RIVUR)

ClinicalTrials.gov ID: NCT00405704

Public ClinicalTrials.gov record NCT00405704. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 4:55 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

In this 2-year, multisite, randomized, placebo-controlled trial involving 607 children with vesicoureteral reflux that was diagnosed after a first or second febrile or symptomatic urinary tract infecton, we evaluated the efficacy of Trimethoprim-Sulfamethoxazole (TMP-SMZ) prophylaxis in preventing recurrences (primary outcome). Secondary outcomes were renal scarring, treatment failure (a composite of recurrences and scarring), and antimicrobial resistance.

Study identification

NCT ID
NCT00405704
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
607 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Months to 71 Months
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2007 (Actual)
Primary completion
Jun 2013 (Actual)
Completion
May 2014 (Actual)
Last update posted
Apr 21, 2020

2007 – 2014

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35233 —
Alfred I. duPont Hospital for Children Wilmington Delaware 19803 —
Children's National Medical Center Washington D.C. District of Columbia 20010 —
Ann & Robert Lurie Children's Hospital of Chicago Chicago Illinois 60614 —
Johns Hopkins School of Medicine Baltimore Maryland 21287 —
Children's Hospital of Boston Boston Massachusetts 02115 —
Children's Hospital of Michigan Detroit Michigan 48201 —
Children's Mercy Hospital Kansas City Missouri 64108 —
Women and Children's Hospital of Buffalo Buffalo New York 14222 —
Wake Forest University Baptist Medical Center Winston-Salem North Carolina 27157 —
Akron Children's Hospital Akron Ohio 44308 —
Cincinnati Children's Hospital Cincinnati Ohio 45229 —
University of Oklahoma Oklahoma City Oklahoma 73104 —
Oregon Health & Science University Portland Oregon 97239 —
Penn State Hershey Medical Center Hershey Pennsylvania 17033 —
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 —
Children's Hospital of Pittsburgh Pittsburgh Pennsylvania 15213 —
Texas Children's Hospital Houston Texas 77030 —
University of Wisconsin Children's Hospital Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00405704, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 21, 2020 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00405704 live on ClinicalTrials.gov.

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