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Study identifier: NCT06083051 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Differences in Postoperative Symptoms With Four Ureteral Stents

Condition: Urinary Stone  ·  Sponsor: University of Wisconsin, Madison

PhaseNA
Planned participants272
Who can joinAll sexes, 18 Years to 89 Years
Healthy volunteersNo

About this study

This is a prospective randomized controlled trial designed to assess the differences in postoperative symptoms related to placement of a 6Fr Percuflex ureteral stents, 6Fr Tria ureteral stents, 4.8Fr Percuflex ureteral stents, and 4.8Fr Tria ureteral stents after ureteroscopy with laser lithotripsy for treatment of upper tract urinary stones. 272 participants will be enrolled and will be on study for up to approximately 10 weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Shuang Li  ·  608.263.8336  ·  lis@urology.wisc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Wisconsin School of Medicine and Public HealthMadison, Wisconsin, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06083051