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A Multi-center, International Prospective Follow up Study

Benign Prostatic Hyperplasia (BPH) Clinical Trial

Official title:
A Multi-center, International Prospective Follow up Study to Assess the Safety and Efficacy of the iTind Procedure After Three to Five Years of Follow Up

Clinical Trial Summary

The study objective is to assess the safety and efficacy of iTind three to five years following treatment.

Clinical Trial Description

This study will recruit patients who participated in the MT-03 study in the iTind arm to assess the safety and efficacy of the iTind procedure at three to five years following treatment as demonstrated by reduction of symptoms measured by IPSS and QoL and improvement of functional parameters as measured by peak urinary flow and PVR. Sexual and erectile function will also be assessed alongside the incidence of any related late occurring adverse events. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04579913
Study type Observational
Source Medi-Tate Ltd.
Contact
Status Terminated
Phase
Start date December 21, 2020
Completion date April 22, 2021
View Details
See also
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