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Diagnostic Test
Quick Renal MRI for Pediatric Kidney Disease
N/A
Recruiting
Led By Ruthie Su, MD
Research Sponsored by University of Wisconsin, Madison
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patient is admitted to American Family Children's Hospital for a febrile UTI, suspected pyelonephritis, or diagnosed pyelonephritis undergoing clinical DMSA scan
History of more than one UTI in the past year
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial proposes a new, faster imaging technique for children with urinary tract problems that is injection-, sedation-, and radiation-free. It could potentially replace current scans and ease the burden of testing for kids with chronic renal disease.
Who is the study for?
This trial is for children and young adults (0-21 years) with kidney conditions like infections or scarring, who are already getting DMSA scans as part of their care. It's not for those uncomfortable with MRI, without signs of infection in urine tests, negative urine cultures, or who can't have an MRI due to other medical reasons.
What is being tested?
The study is testing a new 'quick renal MRI' method against the standard DMSA scan used to detect kidney infections and scarring. The goal is to see if this quick MRI can be a faster, safer option that doesn't need injections, sedation, or radiation.
What are the potential side effects?
Since the quick renal MRI does not use radiation, sedation, or injections unlike traditional imaging methods such as the DMSA scan; it's expected to have fewer risks. However specific side effects aren't listed since MRIs typically don’t involve any.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am in the hospital for a fever and kidney infection, getting a special kidney scan.
Select...
I have had more than one urinary tract infection in the last year.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Sensitivity of Quick MRI as Compared to DMSA scan in Diagnosis of Suspected Acute Pyelonephritis
Sensitivity of Quick MRI as compared to DMSA scan in Diagnosis of Renal Scars
Specificity of Quick MRI as compared to DMSA scan in Diagnosis of Renal Scars
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: DMSA/Quick MRIExperimental Treatment1 Intervention
All participants will go through DMSA and Quick MRI scan to help determine the validity of the Quick Renal MRI in pediatric kidney disease.
Find a Location
Who is running the clinical trial?
University of Wisconsin, MadisonLead Sponsor
1,231 Previous Clinical Trials
3,199,785 Total Patients Enrolled
Ruthie Su, MDPrincipal InvestigatorUniversity of Wisconsin, Madison
Shannon Cannon, MDPrincipal InvestigatorUniversity of Wisconsin, Madison
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am in the hospital for a fever and kidney infection, getting a special kidney scan.I have had more than one urinary tract infection in the last year.You are currently having DMSA scans as part of your regular medical care.Your urine test does not show any signs of infection.I am not comfortable with undergoing a Quick MRI.You cannot have an MRI for medical reasons.Your urine analysis does not show signs of infection.
Research Study Groups:
This trial has the following groups:- Group 1: DMSA/Quick MRI
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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