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Clinical Trial Summary

Robust I study is a feasibility study for evaluating the safety and efficacy of DCB.


Clinical Trial Description

The study is designed to determine the safety and effectiveness for drug coated balloon (DCB). Up to 50 subjects is planned to be enrolled and treated with the study device at up to 5 clinical sites outside of US. Due to significantly higher prevalence of strictures in men vs. women and the etiology of those strictures being different, the study will focus on male subjects with single anterior urethral stricture. Subjects will be followed up post-treatment to one year and then annually for up to 5 years. The annual follow up after the first year is optional. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03014726
Study type Interventional
Source Urotronic Inc.
Contact
Status Completed
Phase Early Phase 1
Start date November 2016
Completion date April 2023

See also
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