Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
MALE
Healthy Volunteers
NCT05698576

TRANBERG® Transperineal MR/US Fusion Laser--Induced Thermal Therapy for Men With Prostate Cancer

Led by Urological Research Network, LLC · Updated on 2023-01-26

20

Participants Needed

1

Research Sites

567 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is set up as a phase I prospective, single center, device interventional pilot study carried in office setting under local anesthesia. It will assess the tolerance and safety of target fusion ablation of prostate cancer tumors using Laser Induced Thermal Therapy (TFA-LITT) guided by fusion imaging in men 50 to 80 years of age with low to intermediate risk prostate cancer Prostate Cancer is currently managed with in a discrete fashion where patients either enroll in active surveillance protocols (No intervention) or undergo full intervention via whole gland treatments - most commonly radical surgery or radiation. These treatments have not shown definitive gains in all cause survival and not uncommonly harbor undesirable adverse effects, most notably: impotency and incontinence. Such events elicit significant and noticeable changes on a male lifestyle and for most prostate cancer tumors are considered overtreatment. This study aims to evaluate the use of TFA-LITT in the office setting under local anesthesia - greatly decreasing patient perioperative surgical risk - focused on the organ sparing cancer lesion ablation, where organ function is preserved. The fundamental objective is to determine the tolerance and safety of TFA-LITT in men with low to intermediate risk prostate cancer, successful performed in the outpatient office-based setting under local anesthesia directed by fusion imaging. Secondary objectives include: 1-Biopsy proven cancer control of ablated areas 12 months after procedure; 2-Uroflowmetry and urinary function Patient Reported Outcome Measures (PROMs) at one, three, six, nine and 12 months; 3- Sexual function Patient Reported Outcome Measures (PROMs) at one, three, six, nine and 12 months; 4- MRI changes of ablated area one, three and 12 months after TFA-LITT; 5- Absence or presence of ejaculation after TFA-LITT.

CONDITIONS

Official Title

TRANBERG® Transperineal MR/US Fusion Laser--Induced Thermal Therapy for Men With Prostate Cancer

Who Can Participate

Age: 50Years - 80Years
MALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing and able to sign informed consent
  • Able and willing to complete all procedures and follow-up visits
  • No urinary retention
  • Prostate volume between 18 and 100 cc by transrectal ultrasound
  • Serum creatinine less than 2 ng/dl and GFR greater than 45
  • Serum PSA less than 20 ng/ml
  • Multiparametric prostate MRI with piRADS scores 3 to 5
  • Prostate volume between 18 and 100 cc by MRI
  • Presence of intermediate risk prostate cancer with tumor volume less than one-third of gland volume by MRI
Not Eligible

You will not qualify if you...

  • Post-void residual volume greater than 250 mL or more than 50% of voided volume
  • Previous prostate cancer treatment such as radiation, brachytherapy, or cryoablation
  • Major neurological diseases including Alzheimer's, Parkinson's, multiple sclerosis, ALS, or spinal cord injury
  • Neurogenic bladder confirmed by urodynamics
  • Use of indwelling Foley catheter or clean intermittent catheterization in prior 30 days
  • Active urinary tract infection
  • SHIM score below 14
  • IPSS score above 23
  • Acute prostatitis
  • Macroscopic hematuria without known cause
  • History of colorectal cancer with anterior perineal rectum resection
  • History of pelvic radiation or radical pelvic surgery
  • History of bladder neck contracture or urethral strictures within 5 years
  • Presence of bladder stones
  • Medical contraindications to TPFLA surgery or local anesthesia
  • Diagnosed or suspected bleeding or clotting disorders such as hemophilia, ITP, or TTP

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Trial Site Locations

Total: 1 location

1

Urology Specialist Group

Hialeah, Florida, United States, 33016

Actively Recruiting

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Research Team

C

Cielo D Guerra, BS

CONTACT

L

Luanda Perez, PA.C

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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