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Clinical Trials/NCT03179228
NCT03179228
Withdrawn
N/A

Phase II, Single Arm Prospective Study To Evaluate Safety And Efficacy Of Prostate Artery Embolization In Patients With Lower Urinary Tract Symptoms Due To Benign Prostatic Hyperplasia

John D Louie1 site in 1 countryOctober 14, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostatic Hyperplasia
Sponsor
John D Louie
Locations
1
Primary Endpoint
Evaluate improvement of symptoms from benign prostatic hyperplasia
Status
Withdrawn
Last Updated
8 years ago

Overview

Brief Summary

The primary study objective is to evaluate improvement of symptoms from benign prostatic hyperplasia (BPH) as assessed by the International Prostate Symptom Score (IPSS) at 12 months post prostatic artery embolization (PAE) with bland microspheres.

Detailed Description

This is a phase II, single center, prospective, single arm, investigational study to evaluate the safety and efficacy of prostate artery embolization (PAE) for treatment of severe lower urinary tract symptoms (LUTS) related to BPH in patients with prostate size greater than 40 grams that either refuse surgical treatment or are considered poor candidates for traditional surgical therapy. Two hundred patients will be enrolled in the single treatment arm with follow-up for no less than 12 months. The study will involve a screening period in which patient eligibility will be determined. Once eligibility is confirmed, patients will receive PAE with bland microspheres within 4 weeks of screening baseline imaging. After treatment, patients will return for follow-up visits at 1 month, 3 months, 6 months, and 12 months post PAE. At each of these visits, patients will complete IPSS and IIEF questionnaires, undergo a physical exam, laboratory assessment (including PSA) and perform a medication review. Repeat TRUS and uroflowmetry will be performed at the 3, 6, and 12 month post PAE follow-up visits. MRI or CT will be conducted at the 3 and 12 month visit. Cystoscopy and proctoscopy will be performed if medically indicated. The primary endpoint will be improvement of BPH symptoms as assessed by the IPSS at 12 months post PAE. Patients will continue to be followed according to the institutional standard of care follow-up schedule after they complete the study. Safety will be evaluated throughout the initial 12 months of the study by assessing adverse events and findings on physical examination. Concomitant medication usage will be assessed.

Registry
clinicaltrials.gov
Start Date
October 14, 2017
End Date
June 1, 2028
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
John D Louie
Responsible Party
Sponsor Investigator
Principal Investigator

John D Louie

Clinical Associate Professor

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Patient is aged 50 years or older.
  • Patient has signed informed consent
  • Patient has experienced lower urinary tract symptoms (LUTS) for at least 6 months prior to study enrollment
  • Patient has a prostate size larger than 40g as measured by MRI or CT (if MR not possible)
  • Patient has an IPSS score greater than or equal to 13
  • Patient either:
  • i. Refuses surgical treatment ii. Is considered high risk for surgical treatment
  • Patient is either:
  • i. Refractory to medical treatment ii. Contraindicated for medical treatment
  • Patient must meet ONE of the following criteria:

Exclusion Criteria

  • Active prostatitis or urinary tract infection
  • History of prostate or bladder cancer, or currently being evaluated for cancer
  • Bladder atonia, neurogenic bladder disorder or other neurological disorder that is impacting bladder function.
  • Urethral stricture, bladder neck contracture, other potentially confounding bladder pathology, bladder disease, or confounding urethral pathology
  • Patient has taken beta blockers, antihistamines, anticonvulsants, or antispasomodics within 1 week of study treatment AND has not been on the same drug dosage for 6 months with a stable voiding pattern.
  • Patient has taken antidepressant, anticholinergics, androgens or gonadotropin-releasing hormonal analogues within 2 months of study treatment AND has not been on the same drug dosage for at least 3 months with a stable voiding pattern.
  • Patient has taken alpha blockers within 4 weeks of study treatment AND has not been on the same drug dosage for at least 3 months with a stable voiding pattern.
  • Patient has taken 5-alpha reductase inhibitors within 3 months of study treatment AND has not been on the same drug for at least 6 months with a stable voiding pattern
  • History of open prostate surgery, radiofrequency, or microwave therapy
  • Previous open bladder or rectosigmoid colon surgery

Outcomes

Primary Outcomes

Evaluate improvement of symptoms from benign prostatic hyperplasia

Time Frame: 12 months

The primary study objective is to evaluate improvement of symptoms from benign prostatic hyperplasia (BPH) as assessed by the International Prostate Symptom Score (IPSS) in a whole number score.

Secondary Outcomes

  • prostate specific antigen (PSA)(12 months)
  • peak urine flow rate (Qmax)(12 months)
  • post-void residual urine volume (PVR)(12 months)
  • Erectile Function Survey(12 months)
  • prostate size(12 months)

Study Sites (1)

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