Libra Medical Inc
Brooklyn Park, Minnesota, 55428, United States
NCT Number: NCT03014726
Robust I study is a feasibility study for evaluating the safety and efficacy of DCB.
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Notify Me18 year and older
Male
Interventional
Early Phase 1
Brooklyn Park, Minnesota, 55428, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Urotronic Drug Coated Balloon (DCB) is a catheter with a tapered atraumatic tip. The distal end of the catheter has a semi-compliant inflatable balloon coated with a proprietary coating containing the drug and carriers.
Time frame: 90 days post-procedure
Time frame: 90 days post-procedure
Urotronic Inc.
Industry
ROBUST I Pilot Study, ROBUST I Study, Re-Establishing Flow Via Drug Coated Balloon For The Treatment Of Urethral Stricture Disease
Acronym: ROBUST
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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