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Ureteral Stent
RELIEF stent placement for Ureteral Obstruction
N/A
Waitlist Available
Led By Kyle Scarberry, MD
Research Sponsored by University Hospitals Cleveland Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Ureteral stone of 5-25 mm measured on plain abdomen X-ray KUB (Kidney Ureter Bladder) or CT (computed tomography).
Upper or middle third ureteral stricture.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 0-30 days.
Awards & highlights
Study Summary
This trial will test a new type of ureteral stent that is thinner and may reduce bladder irritative symptoms and urinary reflux.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 0-30 days.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~0-30 days.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Loin Pain Scores From Baseline
Incidence of Bladder Irritation Symptoms (e.g. Frequency, Urgency, Nocturia, Urine Leakage...) Associated With the RELIEF Stent.
Secondary outcome measures
Incidence of RELIEF Stent-Related Adverse Events
Trial Design
1Treatment groups
Experimental Treatment
Group I: RELIEF stent placementExperimental Treatment1 Intervention
After meeting the inclusion criteria and being consented, patients will have the RELIEF stent inserted in the ureter during cystoscopy per standard of care for ureteral stent placement.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
RELIEF Stent
2021
N/A
~30
Find a Location
Who is running the clinical trial?
University Hospitals Cleveland Medical CenterLead Sponsor
317 Previous Clinical Trials
340,330 Total Patients Enrolled
Kyle Scarberry, MDPrincipal Investigator - University Hospitals Cleveland Medical Center
University Hospitals Cleveland Medical Center
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