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Urinary Sensor for Cystourethrography

NCT00547820 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2009-10-28

No results posted yet for this study

Summary

Evaluation of urinary sensor that will be activated by the urine during voiding cystourethrography in pediatric patients

Conditions

  • Radiation Dose During VCUG

Interventions

OTHER

placebo

DEVICE

Urinary sensor

Sponsors & Collaborators

  • Rambam Health Care Campus

    lead OTHER

Principal Investigators

  • Olga R Brook, MD · Department of Diagnostic Imaging, Rambam Health Care Campus

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
1 Month
Max Age
10 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-07-31
Primary Completion
2008-06-30
Completion
2008-06-30

Countries

  • Israel

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00547820 on ClinicalTrials.gov