Status:
RECRUITING
Differences in Postoperative Symptoms With Four Ureteral Stents
Lead Sponsor:
University of Wisconsin, Madison
Conditions:
Urinary Stone
Eligibility:
All Genders
18-89 years
Phase:
NA
Brief Summary
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 ...
Detailed Description
The investigators will compare Ureteral Stent Symptom Questionnaire (USSQ) scores with each ureteral stent. Laser lithotripsy is a surgical procedure performed during stone surgeries. The Percuflex ur...
Eligibility Criteria
Inclusion
- Patients with renal or ureteral urinary stones who require endoscopic treatment and stent placement in the outpatient operating room.
Exclusion
- Pregnant patients
- Patients with transplant kidneys
- Patients with irreversible coagulopathy
- Patients with known ureteral stricture disease
- Non-English speaking, vulnerable patients such as lacking of decision-making capability, prisoner, adult unable to consent, will not be enrolled.
- Patients with planned staged procedures.
- Patients who have stent placed before surgery.
Key Trial Info
Start Date :
March 21 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2026
Estimated Enrollment :
272 Patients enrolled
Trial Details
Trial ID
NCT06083051
Start Date
March 21 2024
End Date
December 1 2026
Last Update
June 6 2025
Active Locations (1)
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1
University of Wisconsin School of Medicine and Public Health
Madison, Wisconsin, United States, 53792