Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01775488

Safety and Initial Efficacy Study of the Vortx Rx for Treatment of Benign Prostatic Hyperplasia (Canada)

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
HistoSonics, Inc. · Industry
Sex
Male
Age
50 Years
Healthy volunteers
Not accepted

Summary

The HistoSonics' Histotripsy BPH Device, the Vortx Rx, is a portable ultrasound therapy device. The purpose of this study is to assess and monitor the performance of the Vortx Rx for initial safety and efficacy for the treatment of Benign Prostatic Hyperplasia.

Conditions

Interventions

TypeNameDescription
DEVICEVortx Rx - Histotripsy BPH DeviceNon-invasive histotripsy treatment / therapy to be delivered by surgeon using very low duty cycle ultrasound pulses from outside the patient's body. These pulses form a bubble cloud at the focal area within the prostate which mechanically breaks up the cellular structure of the soft tissue. During treatment, a surgeon is able to direct the bubble cloud throughout the targeted volume using controls located on the device console and using the real-time ultrasound for visualization feedback and control of the bubble cloud location.

Timeline

Start date
2013-06-01
Primary completion
2014-06-01
First posted
2013-01-25
Last updated
2015-08-19

Source: ClinicalTrials.gov record NCT01775488. Inclusion in this directory is not an endorsement.