The Edison System for Treatment of Benign Prostatic Hyperplasia (BPH) Using Histotripsy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age50+
SponsorHistoSonics, Inc.

About this trial

The purpose of this trial is to evaluate the safety of histotripsy using the HistoSonics Edison System for treatment of BPH.

Eligibility criteria

Qualifiers

Subject is ≥ 50 years of age.

Subject has signed the Ethics Committee (EC) approved trial Informed Consent Form (ICF) prior to any trial related tests/procedures and is willing to comply with trial procedures and required follow-up assessments.

Subject is diagnosed with BPH.

Subject has a Body Mass Index (BMI) < 27.

Disqualifiers

Subject has a life expectancy of less than one (1) year.

Subject has a known sensitivity to contrast media and cannot be adequately pre-medicated.

Subject has a post-void residual ≥ 150 mL confirmed via ultrasound.

Subject has an estimated glomerular filtration rate (eGFR) ≤ 50 mL/min, ≤ 14 days prior to the planned index procedure date.

Trial design

Treatments tested in this trial

  • HistoSonics Edison System

Treatment groups

80 Participants
are divided into 1 treatment group

Sponsors and collaborators