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Clinical Trials in the USA / NCT06312722
Recruiting Not applicable

Safety and Effectiveness of the Optilume® BPH Catheter System in a Post-Market Study

NCT06312722 · tracked via the Priya Life Science USA tracker
Sponsor
Urotronic Inc.
Phase
Not applicable
Started
2024-02-07
Last updated
2026-07-10

Condition(s) studied

Benign Prostatic Hyperplasia

Investigational drug(s) / intervention(s)

Optilume® BPH Catheter System

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.

Study summary

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

Eligibility

Sex
MALE
Min age
50 Years
Max age
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (7)

FacilityCityRegionStatus
Arkansas Urology Little Rock Arkansas Recruiting
Florida Urology Partners, LLP Tampa Florida Recruiting
Ochsner LSU Health Shreveport - Regional Urology Shreveport Louisiana Recruiting
Sheldon Freedman MD, Ltd Las Vegas Nevada Recruiting
Oregon Urology Institute Springfield Oregon Recruiting
Midtown Urology Associates Austin Texas Recruiting
Houston Methodist Urology Associates Houston Texas Recruiting

More Urotronic Inc. trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06312722 on ClinicalTrials.gov ↗ ← All trials in the USA