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Post-Market Study to Assess iTind Safety in Comparison to UroLift — MT-08  

Benign Prostatic Hyperplasia (BPH) Clinical Trial

Official title:
A Post-Market, Prospective, Randomized, Controlled, Multicenter International Study to Assess the Safety of the Temporarily Implanted Nitinol Device (iTind) Compared to the UroLift® System in Subjects With Symptomatic Benign Prostatic Hyperplasia (BPH)

Clinical Trial Summary

The study objective is to evaluate the safety of the iTind device comparied to UroLift.

Clinical Trial Description

UroLift is a treatment for relieving lower urinary tract symptoms (LUTS) secondary to benign Prostatic Hyperplasia (BPH) as a minimally invasive procedure. This procedure has proven to have high efficacy with regards to improving objective and subjective parameters. The iTind is a minimally invasive temporary device designed to relieve LUTS secondary to BPH. This study is designed to compare the minimally invasive iTind device to UroLift. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04757116
Study type Interventional
Source Olympus Corporation of the Americas
Contact Selen ZuelbaharOlgun, PhD
Phone 1-650-586-2171
Email Selen.ZuelbaharOlgun@olympus.com
Status Recruiting
Phase N/A
Start date September 26, 2022
Completion date December 31, 2030
View Details
See also
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