PROARTE -PROstate ARTery to Reduce the Symptoms of Benign Prostatic Hyperplasia (PROARTE)

This is an interventional treatment trial for Benign Prostatic Hyperplasia focused on measuring Prostate artery embolization, Benign Prostatic Hyperplasia, Lower Urinary Tract Symptoms, Quality of Life Read More

Inclusion Criteria:

• • Men ≥45 and ≤90 years presenting with benign prostatic hyperplasia with symptoms for at least 6 months that are refractory to medical management or in whom medications are contraindicated, not tolerated, or refused.

  • International Prostate Symptom Score (I-PSS) score 14 or greater.
  • Quality of Life (QoL) score ≥ 3
  • Peak urinary flow (Qmax) less than or equal to 12 mL/s with void volume >125mL.
  • Prostate volume greater than 30 cc as determined by ultrasound, MRI, or CT.
  • Personal risk <40% based on the University of Texas San Antonio prostate cancer risk calculator or having a negative prostate biopsy for cancer within the last 24 months.
  • Able to provide written consent.
  • Not participating in any other investigational drug or device studies.

Exclusion Criteria:

• • History of biopsy-proven prostate cancer

  • Renal insufficiency (glomerular filtration rates (GFR) less than 40mL/min/1.73 m2 who are not already on dialysis)
  • Prior prostate surgery or intervention, including trans-urethral resection of the prostate, balloon dilation, stent implantation, laser prostatectomy, radiation, UroLift®, or hyperthermia
  • Other bladder or urethral pathology requiring therapy, either in the past or currently, including neurogenic bladder, sphincteric abnormalities, bladder cancer, or other causes of bladder atonia.
  • Other causes of urinary obstruction, such as strictures of urethra or ureters, not related to BPH
  • Current decompensated congestive heart failure, uncontrolled diabetes mellitus, significant respiratory disease, or known immunosuppression.
  • Neurological disease, including multiple sclerosis, amyotrophic lateral sclerosis, Parkinson's disease, and previous spinal nerve surgery
  • Patients with platelet count <50,000/μL or International Normalized Ratio (INR) >1.8, unless corrected for the procedure
  • Active urinary tract infection. Patients must have a negative culture within 7 days of the procedure.
  • Allergy to iodinated contrast agents unless pre-treated by corticosteroids.
  • Acute urinary retention.
  • Post void residual (PVR) > 250 mL with urodynamic evidence of atonic bladder. Patients with a PVR >250 but urodynamic testing consistent with obstruction will be allowed.
  • Bladder stone within three months prior to the procedure.
  • Hematuria not evaluated by Urologist for causes other than BPH.
  • Previous rectal surgery (excluding hemorrhoidectomy) or history of rectal disease.
  • Prior pelvic irradiation or radical pelvic surgery.

Imaging exclusion criteria:

• Internal iliac artery occlusion as determined by either CT or MRI.