Sponsor:
Urotronic Inc.
Code:
NCT06312722
Conditions
Benign Prostatic Hyperplasia
Eligibility Criteria
Sex: Male
Age: 50+
Healthy Volunteers: Not accepted
Interventions
Optilume® BPH Catheter System
Brief summary:
Conditions
Benign Prostatic Hyperplasia
Study ID
NCT06312722
Start date
Feb 7, 2024
Status verified date
Jul, 2026
Completion date
Feb 7, 2031
Anticipated
Primary completion date
Feb 7, 2031
Anticipated
Eligibility Criteria
Sex: Male
Age: 50+
Healthy Volunteers: Not accepted
Enrollment
92 participants
Anticipated
Intervention Model
Single group
Primary purpose
Treatment
Arms
other: Study Arm
Interventions
Optilume® BPH Catheter System
Primary outcome measure
Central contacts
Steve Madej
smadej@laborie.comLocations
Arkansas Urology
Recruiting
Little Rock, Arkansas, United States, 72211
Contacts
Principal Investigator:
Jeffrey Marotte, MD
Florida Urology Partners, LLP
Recruiting
Tampa, Florida, United States, 33615
Contacts
Principal Investigator:
Osvaldo Padron, MD
Ochsner LSU Health Shreveport - Regional Urology
Recruiting
Shreveport, Louisiana, United States, 71106
Contacts
Principal Investigator:
Jared Moss, MD
Sheldon Freedman MD, Ltd
Recruiting
Las Vegas, Nevada, United States, 89144
Contacts
Principal Investigator:
Sheldon Freedman, MD
Oregon Urology Institute
Recruiting
Springfield, Oregon, United States, 97477
Contacts
Principal Investigator:
David DiMarco, MD
Midtown Urology Associates
Recruiting
Austin, Texas, United States, 78705
Contacts
Principal Investigator:
Michael Trotter, MD
Houston Methodist Urology Associates
Recruiting
Houston, Texas, United States, 77030
Contacts
Principal Investigator:
Ricardo Gonzalez, MD
Sponsor
Urotronic Inc.
Last update posted
Jul 10, 2026
Last verified
Jul, 2026
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Urotronic Inc. on 2026-07-10.