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Clinical Trial Summary

This multi-center trial is being completed to compare patient outcomes related to the Imajin silicone stent in comparison to non-silicone polyurethane stents after ureteroscopy. Eligible participants will be enrolled and randomly assigned to receive the Imajin silicone stent or a non-silicone stent. In addition, the participants will complete questionnaires and have follow-up information collected (approximately 60 days after surgery). The trial hypothesizes that a ureteral stent made of silicone, will have superior outcomes when compared to non-silicone stents.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05026710
Study type Interventional
Source University of Michigan
Contact Elaina Shoemaker
Phone 734-764-3916
Email esekulos@med.umich.edu
Status Recruiting
Phase N/A
Start date December 2, 2021
Completion date December 2024

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