Prospective Controlled Randomized Study of PAE vs TURP for BPH Treatment.

Not Applicable

Withdrawn

• Conditions: Benign Prostatic Hyperplasia
• Interventions: Procedure: PAE; Procedure: TURP; Device: Bipolar electrosurgery generator; Device: Gelatin microspheres

• Registration Number: NCT02566551
• Lead Sponsor: Group of Research in Minimally Invasive Techniques

Brief Summary

The purpose of this prospective randomized controlled study is to compare the improvement of symptoms from benign prostatic hyperplasia (BPH) and the improvement of QoL, in patients undergoing prostatic artery embolization (PAE) or conventional transurethral resection of the prostate (TURP).

Detailed Description

The purpose of this prospective randomized controlled study is to compare the improvement of symptoms from benign prostatic hyperplasia (BPH) as assessed by the International Prostate Symptom Score (IPSS) and the improvement of QoL assessed by QoL questionnaire in patients undergoing prostatic artery embolization (PAE) to patients of similar characteristics undergoing conventional transurethral resection of the prostate (TURP).

Study Timeline

• Study First Submitted: 2015-08-10
• Study Start: 2015-10
• Study First Submitted QC: 2015-10-01
• Study First Posted: 2015-10-02
• Primary Completion: 2018-05
• Study Completion: 2019-05
• Status Verified: 2019-07
• Last Update Submitted: 2019-07-11
• Last Update Posted: 2019-07-12

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

Patients evaluated in the Urology Service because of BPH, candidate to TURP.

• Signed informed consent

• Lower urinary tract symptoms (LUTS) secondary to BPH for at least 6 months prior to study AND/OR baseline IPSS Score > 13 AND/OR acute urinary retention with impossibility to remove urinary catheter AND/OR BPH symptoms refractory to medical treatment or for whom medication is contraindicated, not tolerated or refused Prostate size of at least 50 grams measured by MRI

• Patient must meet ONE of the following criteria:

  1. Baseline Prostate Specific Antigen (PSA) <4 ng/mL (no prostate biopsy required)
  2. Baseline PSA >4 ng/mL and ≤10 ng/mL AND free PSA > 15% of total PSA (no prostate biopsy required)
  3. Baseline PSA >4 ng/mL and ≤10 ng/mL AND free PSA <15% of total PSA AND a negative prostate biopsy result (minimum 12 core biopsy)
  4. Baseline PSA >10 ng/mL AND a negative prostate biopsy (minimum 12 core biopsy)

Exclusion Criteria

• Active urinary tract infection

• Patients with cystoscopy findings suspicious for bladder cancer must undergo biopsy and have a negative histopathology report to be enrolled in the study

• Biopsy proven prostate or bladder cancer

• The following patients must undergo prostate biopsy with a minimum of 12 cores and have a negative histopathology report to be enrolled in the study:

  • Patients with digital rectal examination (DRE) findings suspicious for prostate cancer
  • Patients with baseline PSA levels > 10 ng/mL
  • Patients with baseline PSA levels >4 ng/mL and < 10 ng/mL AND free PSA < 15% of total PSA

• Bladder atonia, neurogenic bladder disorder or other neurological disorder that is impacting bladder function (eg multiple sclerosis, Parkinson's disease, spinal cord injuries, etc)

• Urethral stricture, bladder neck contracture, sphincter abnormalities, urinary obstruction due to causes other than BPH, or other potentially confounding bladder or urethral disease or condition

• Allergy to iodinated contrast agents

• Hypersensitivity to gelatin products

• Previous non-medical BPH treatment, including surgery, TURP, needle ablation, microwave or laser therapy, balloon dilation, stent implantation, or any other invasive treatment to the prostate

• Known major iliac arterial occlusive disease or any known condition that catheterization of the prostatic arteries or is a contraindication to embolization, as vasospasm, anatomical variations that imply a risk of embolization, bleeding, prostatic arteries diameter inferior to microcatheter profile, pelvic inflammatory disease

• Contraindication to magnetic resonance imaging

• History of prostatitis in the last 5 years, not totally controlled with medical treatment

• History of pelvic irradiation or radical pelvic surgery

• Coagulation disturbances not normalized by medical treatment

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Prostate artery embolization	PAE	Prostatic artery embolization (PAE) To perform embolization, gelatin microspheres (300-500 microns) will be used in this arm
Transurethral resection of the prostate	Bipolar electrosurgery generator	Transurethral resection of the prostate (TURP) A bipolar electrosurgery generator will be used to perform TURP
Transurethral resection of the prostate	TURP	Transurethral resection of the prostate (TURP) A bipolar electrosurgery generator will be used to perform TURP
Prostate artery embolization	Gelatin microspheres	Prostatic artery embolization (PAE) To perform embolization, gelatin microspheres (300-500 microns) will be used in this arm

Primary Outcome Measures

Name	Time	Method
Improvement of symptoms	12 months	Improvement (change) of symptoms assessed by IPSS Score (International Prostate Symptom Score )

Secondary Outcome Measures

Name	Time	Method
Improvement in QoL	12 months	Improvement (change) of quality of life assessed by QoL score
Duration of hospitalization post procedure	3 weeks	Number of days of postprocedure hospitalization
Preservation of erectile function	12 months	Change from baseline in erectile function using the International Index of Erectile Function (IIEF)

Trial Locations

Locations (1)

Hospital Universitario Lozano Blesa; 🇪🇸 Zaragoza, Spain