Recruiting

Optilume® BPH

Sponsor:

Urotronic Inc.

Code:

NCT06312722

Conditions

Benign Prostatic Hyperplasia

Eligibility Criteria

Sex: Male

Age: 50+

Healthy Volunteers: Not accepted

Interventions

Optilume® BPH Catheter System

Study Details

Brief summary:

The goal of this clinical trial is to verify the continued safety and effectiveness for the Optilume BPH Catheter System.

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

Eligibility Criteria

Sex: Male

Age: 50+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Male subject ≥ 50 years old
2. Diagnosed with lower urinary tract symptoms (LUTS) secondary to obstructive benign prostatic hyperplasia (BPH)
3. Able to be treated with the Optilume BPH Catheter System in accordance with the Instructions for Use
4. Prostate volume < 80 g with a prostatic urethral length between 32-55 mm as determined by trans-rectal ultrasound (TRUS)
5. International Prostate Symptom Score (IPSS) ≥ 13
6. Peak urinary flow rate (Qmax) 5-15 mL/sec with minimum voided volume of 125 mL
7. Willing to provide informed consent and comply with protocol required follow-up

Exclusion Criteria:

1. Unwilling to abstain from sexual intercourse or use a condom for 30 days post-procedure and utilize a highly effective contraceptive for at least 12 months post-procedure
2. Presence of an artificial urinary sphincter, penile prosthesis, or stent(s) in the urethra or prostate
3. Any prior minimally invasive intervention (e.g., TUNA, Balloon, Microwave, Rezūm, UroLift) or surgical intervention of the prostate
4. Confirmed or suspected malignancy of prostate or bladder. Negative prostate biopsy required within 6 months of enrollment if PSA at baseline is > 4 ng/mL with free PSA < 25%.
5. Active urinary tract infection (UTI) confirmed by culture
6. Neurogenic bladder or sphincter abnormalities or neurological disorders that might affect bladder or sphincter function
7. History of overt urinary incontinence requiring the use of pads
8. Previous or current diagnosis of urethral strictures, bladder neck contracture or detrusor muscle spasms
9. Current post-void residual volume (PVR) > 300 mL or catheter dependent bladder drainage
10. Known poor detrusor muscle function (e.g., Qmax < 5 mL/sec)
11. Active bladder, ureteral, or urethral stones or stone passage within the last 3 months
12. Current poorly controlled diabetes (i.e., hemoglobin A1c ≥ 8%)
13. Anatomy (e.g., presence of false passage or size of meatus) is not suitable for treatment with the Optilume BPH Catheter System
14. Obstructive median lobe in the opinion of the investigator

Study Design

Enrollment

92 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

other: Study Arm

Optilume BPH Catheter System

Interventions

Optilume® BPH Catheter System

The Optilume BPH Catheter System is a combination drug/device minimally invasive surgical therapy (MIST) comprised of an uncoated pre-dilation balloon catheter and a separate drug coated balloon (DCB) catheter. The distal end of each catheter has a semi-compliant, inflatable, double lobe balloon that is used to dilate the prostate. The double-lobe DCB catheter is coated with a proprietary coating containing the active pharmaceutical agent paclitaxel. The drug coating covers the working length of the balloon body.

Primary outcome measure

  • Change in International Prostate Symptom Score (IPSS) [ Time Frame: Baseline to 12 months ]
  • Rate of a composite of treatment-related serious adverse events (SAEs) [ Time Frame: 3 months ]

Central Contacts and Locations

Central contacts

Locations

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

More Information

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.