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

Description

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 Overview

Study Details

Study overview

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

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

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

Condition
Benign Prostatic Hyperplasia
Intervention / Treatment

-

Contacts and Locations

Little Rock

Arkansas Urology, Little Rock, Arkansas, United States, 72211

Tampa

Florida Urology Partners, LLP, Tampa, Florida, United States, 33615

Shreveport

Ochsner LSU Health Shreveport - Regional Urology, Shreveport, Louisiana, United States, 71106

Las Vegas

Sheldon Freedman MD, Ltd, Las Vegas, Nevada, United States, 89144

Austin

Midtown Urology Associates, Austin, Texas, United States, 78705

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • 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

Ages Eligible for Study

50 Years to

Sexes Eligible for Study

MALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Urotronic Inc.,

Steven Kaplan, MD, FACS, PRINCIPAL_INVESTIGATOR, Professor of Urology

Study Record Dates

2031-02-07