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

Primary Purpose

Benign Prostatic Hyperplasia

Status
Withdrawn
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
PAE
Gelatin microspheres
TURP
Bipolar electrosurgery generator
Sponsored by
Group of Research in Minimally Invasive Techniques
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Benign Prostatic Hyperplasia focused on measuring Prostatic artery embolization, Transurethral resection of the prostate

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

Sites / Locations

  • Hospital Universitario Lozano Blesa

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Prostate artery embolization

Transurethral resection of the prostate

Arm Description

Prostatic artery embolization (PAE) To perform embolization, gelatin microspheres (300-500 microns) will be used in this arm

Transurethral resection of the prostate (TURP) A bipolar electrosurgery generator will be used to perform TURP

Outcomes

Primary Outcome Measures

Improvement of symptoms
Improvement (change) of symptoms assessed by IPSS Score (International Prostate Symptom Score )

Secondary Outcome Measures

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

Full Information

First Posted
August 10, 2015
Last Updated
July 11, 2019
Sponsor
Group of Research in Minimally Invasive Techniques
Collaborators
Hospital Clínico Universitario Lozano Blesa, Universidad de Zaragoza
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1. Study Identification

Unique Protocol Identification Number
NCT02566551
Brief Title
Prospective Controlled Randomized Study of PAE vs TURP for BPH Treatment.
Official Title
Prospective Controlled Randomized Study of Prostatic Arteries Embolization (PAE) vs Transurethral Resection of the Prostate (TURP) for Benign Prostatic Hyperplasia (BPH) Treatment.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Withdrawn
Study Start Date
October 2015 (Actual)
Primary Completion Date
May 2018 (Anticipated)
Study Completion Date
May 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Group of Research in Minimally Invasive Techniques
Collaborators
Hospital Clínico Universitario Lozano Blesa, Universidad de Zaragoza

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostatic Hyperplasia
Keywords
Prostatic artery embolization, Transurethral resection of the prostate

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prostate artery embolization
Arm Type
Experimental
Arm Description
Prostatic artery embolization (PAE) To perform embolization, gelatin microspheres (300-500 microns) will be used in this arm
Arm Title
Transurethral resection of the prostate
Arm Type
Active Comparator
Arm Description
Transurethral resection of the prostate (TURP) A bipolar electrosurgery generator will be used to perform TURP
Intervention Type
Procedure
Intervention Name(s)
PAE
Other Intervention Name(s)
Prostate artery embolization, Prostate arteries embolization, Embolization of the prostate, Prostatic artery embolization
Intervention Description
Embolization of the prostate with gelatin embolization spheres via microcatheterization of the prostatic arteries.
Intervention Type
Device
Intervention Name(s)
Gelatin microspheres
Other Intervention Name(s)
Embolization microspheres
Intervention Description
Gelatin embolization microspheres (300-500 microns) will be used as embolic material for the prostatic artery embolization (PAE) protocol
Intervention Type
Procedure
Intervention Name(s)
TURP
Other Intervention Name(s)
Transurethral resection of the prostate, Transurethral prostatic resection
Intervention Description
Bipolar transurethral resection of the prostate
Intervention Type
Device
Intervention Name(s)
Bipolar electrosurgery generator
Other Intervention Name(s)
Transurethral prostatic resection
Intervention Description
A bipolar electrosurgery generator will be used to perform transurethral resection of the prostate (TURP)
Primary Outcome Measure Information:
Title
Improvement of symptoms
Description
Improvement (change) of symptoms assessed by IPSS Score (International Prostate Symptom Score )
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Improvement in QoL
Description
Improvement (change) of quality of life assessed by QoL score
Time Frame
12 months
Title
Duration of hospitalization post procedure
Description
Number of days of postprocedure hospitalization
Time Frame
3 weeks
Title
Preservation of erectile function
Description
Change from baseline in erectile function using the International Index of Erectile Function (IIEF)
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Maximum urinary flow rate
Description
Change from baseline in maximum urinary flow rate (Qmax)
Time Frame
12 months
Title
Post-void residual urinary volume
Description
Change from baseline in post-void residual urinary volume (PVR)
Time Frame
12 months
Title
Detrusor pressure
Description
Change from baseline in detrusor pressure (Pdet)
Time Frame
12 months
Title
Mean prostate volume
Description
Change from baseline in mean prostate volume, as determined by transrectal US
Time Frame
12 months
Title
Structural and morphological changes in MRI
Description
Change from baseline in mean prostate volume, and structural and morphological changes as determined by MRI
Time Frame
12 months
Title
Prostate specific antigen
Description
Change from baseline in prostate specific antigen (PSA)
Time Frame
12 months
Title
Overall adverse events
Description
Overall adverse events
Time Frame
12 months
Title
Procedure related adverse events
Description
Procedure related adverse events
Time Frame
12 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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: Baseline Prostate Specific Antigen (PSA) <4 ng/mL (no prostate biopsy required) Baseline PSA >4 ng/mL and ≤10 ng/mL AND free PSA > 15% of total PSA (no prostate biopsy required) 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) 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Miguel A De Gregorio, PhD
Organizational Affiliation
University of Zaragoza. Chairman of Radiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Lozano Blesa
City
Zaragoza
ZIP/Postal Code
50003
Country
Spain

12. IPD Sharing Statement

Learn more about this trial

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

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