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Results of Selective Prostatic Arterial Embolization in Patients With Indwelling Urinary Catheter Due to Benign Prostatic Hyperplasia Refractory to Medical Treatment. (Prost-EMBOL)

Primary Purpose

Benign Prostatic Hyperplasia

Status
Terminated
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Prostatic arterial embolization using BeadBlock (Terumo)
Sponsored by
University Hospital, Rouen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Benign Prostatic Hyperplasia

Eligibility Criteria

50 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with a urinary retention due to obstructive benign prostatic hyperplasia (BPH) confirmed by endoscopy,
  • Patients aged 50-85 years,
  • Patients with indwelling urinary catheter for at least 1 month,
  • Patients with at least one failure of a trial without catheter despite alpha-blocker treatment for at least 72 hours,
  • Patients informed about alternative treatment (transurethral resection of the prostate, laser prostatectomy, prostatic adenomectomy),
  • Patients signed an informed consent form.

Exclusion Criteria:

  • Prostate cancer (evaluated by PSA, physical examination, in all patients and by prostatic biopsy in suspicious cases).
  • History of relevant neurological disease (e.g. multiple sclerosis, spinal cord injury, parkinson's disease).
  • Patients who have on urodynamic investigation evidence of an atonic bladder.
  • Urethral stricture
  • Chronic persistent local pathology that may cause urinary symptoms (e.g. interstitial cystitis, tumor, bladder stone).
  • Renal insufficiency stade 3 or 4 (creatinine clearance < 35 mL/min)
  • Any allergy or contraindication to ciprofloxacin or drugs used in this protocole (xylocaine, Atarax, paracetamol, and nonsteroidal anti-inflammatory drug)
  • Any allergy to intravenous contrast agent or iodine
  • Thyrotoxicosis
  • Concomitant use of tizanidine
  • Patients participating to another research protocol

Sites / Locations

  • Rouen University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Embolization procedure

Arm Description

selective prostatic arterial embolization using BeadBlock (Terumo) particules

Outcomes

Primary Outcome Measures

Procedural Success
Procedural success was defined as cessation of extravasation and/or occlusion of the targeted vessel on postembolization arteriography. Voiding diary : mictirution volume and postvoid residual volume measurements by ultrasonography

Secondary Outcome Measures

success of the procedure : ability to urinate after their catheter
Ablation of Indwelling Urinary Catheter
success of the procedure : ability to urinate after their catheter
Ablation of Indwelling Urinary Catheter
success of the procedure : ability to urinate after their catheter
Ablation of Indwelling Urinary Catheter

Full Information

First Posted
July 4, 2013
Last Updated
July 29, 2015
Sponsor
University Hospital, Rouen
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1. Study Identification

Unique Protocol Identification Number
NCT01931605
Brief Title
Results of Selective Prostatic Arterial Embolization in Patients With Indwelling Urinary Catheter Due to Benign Prostatic Hyperplasia Refractory to Medical Treatment.
Acronym
Prost-EMBOL
Official Title
Results of Selective Prostatic Arterial Embolization in Patients With Indwelling Urinary Catheter Due to Benign Prostatic Hyperplasia Refractory to Medical Treatment.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Terminated
Why Stopped
Enrolling participants has halted prematurely and will not resume due to the Departure of the principal investigator
Study Start Date
May 2014 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Rouen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Patients with indwelling urinary catheter for chronic retention due to obstructive BPH refractory to medical therapy are candidates for prostatectomy still considered as the gold standard of treatment. Urinary tract infection, strictures, postoperative pain, incontinence, sexual dysfunction, anesthesiologist risk and blood loss are complications associated with surgery. Minimally invasive treatments were originally conceived as an attempt to offer equivalent efficacy without the burden and risk of operative morbidity. Recently, it was suggested that prostatic arterial embolization (PAE) to treat BPH might follow uterine artery embolization for uterine leiomyomas. Animal studies in pigs and dogs have shown that PAE is safe and can induce prostatic volume reduction. The first report of this technique in the management of BPH in humans was by DeMeritt et al, who reported a single case of BPH with obstructive symptoms and blood loss refractory to other treatments that was successfully managed by PAE with polyvinyl alcohol (PVA) particles. Objective : We investigate whether PAE might be a feasible procedure as an alternative treatment option to treat urinary retention due to obstructive BPH. The primary objective is to evaluate the success rate of procedure defined when selective prostatic arterial catheterization and embolization were achieve and patients can be able to urinate after their urinary catheter has been removed. Patients and methods : A monocentric prospective study is undertaken in 25 patients aged 50-85 years who present with indwelling urinary catheter due to obstructive BPH refractory to medical treatment with a clinical indication for surgery who agreed to undergo PAE. The study is approved by the hospital ethical committee and an informed consent form for PAE as an alternative treatment is signed by all participants. Statistical analysis : The sample size has been calculated in order to have an estimated probability of success (corresponding of primary objective) of 50% (worst case) with 95% confidence intervals of 30 to 70. The two-sample t-test (and Wilcoxon rank-sum test) is used to compare the mean changes of the variables from baseline to 10, 30 and 90 days. Finally, the Chi-square test is used to test for adverse events at the end of follow-up. P ≤ 0.05 is indicative of statistically significant.
Detailed Description
Embolization is performed under local anesthesia in one day surgery unit by unilateral approach, usually the right femoral artery. Initially, pelvic angiography is performed to evaluate the iliac and prostatic arteries. Then, a 5-F catheter is introduced in right femoral artery to catheterize the left hypogastric artery and reach its anterior division. The inferior vesical artery and finally the prostatic vessels are selectively catheterized with a 3-F coaxial microcatheter. For embolization, nonspherical 100-300 μm PVA particles is used. The endpoint chosen for embolization is slow flow or near-stasis in the prostatic vessels with interruption of the arterial flow and prostatic gland opacification. When embolization of the left prostatic arteries was finished, the right prostatic arteries were embolized in the same way. Urinary catheter is removed 10 days after the embolization procedure. Voiding trials is performed and the successfull urination after urethral catheter removal is defined as three consecutive spontaneous micturitions with postvoid residual less than 100% of each micturition volume. If the patient is unable to urinate, a urethral catheter will replace before hospitalization discharge and the patient will return to our outpatient clinic for another voiding trial until the end of protocol. Assessments were carried out 10, 30 and 90 days after initial embolization allocation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostatic Hyperplasia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Embolization procedure
Arm Type
Experimental
Arm Description
selective prostatic arterial embolization using BeadBlock (Terumo) particules
Intervention Type
Device
Intervention Name(s)
Prostatic arterial embolization using BeadBlock (Terumo)
Intervention Description
Selective Prostatic arterial embolization using BeadBlock (Terumo)particuls
Primary Outcome Measure Information:
Title
Procedural Success
Description
Procedural success was defined as cessation of extravasation and/or occlusion of the targeted vessel on postembolization arteriography. Voiding diary : mictirution volume and postvoid residual volume measurements by ultrasonography
Time Frame
Day 1
Secondary Outcome Measure Information:
Title
success of the procedure : ability to urinate after their catheter
Description
Ablation of Indwelling Urinary Catheter
Time Frame
Day 10
Title
success of the procedure : ability to urinate after their catheter
Description
Ablation of Indwelling Urinary Catheter
Time Frame
Day 90
Title
success of the procedure : ability to urinate after their catheter
Description
Ablation of Indwelling Urinary Catheter
Time Frame
Day 30

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a urinary retention due to obstructive benign prostatic hyperplasia (BPH) confirmed by endoscopy, Patients aged 50-85 years, Patients with indwelling urinary catheter for at least 1 month, Patients with at least one failure of a trial without catheter despite alpha-blocker treatment for at least 72 hours, Patients informed about alternative treatment (transurethral resection of the prostate, laser prostatectomy, prostatic adenomectomy), Patients signed an informed consent form. Exclusion Criteria: Prostate cancer (evaluated by PSA, physical examination, in all patients and by prostatic biopsy in suspicious cases). History of relevant neurological disease (e.g. multiple sclerosis, spinal cord injury, parkinson's disease). Patients who have on urodynamic investigation evidence of an atonic bladder. Urethral stricture Chronic persistent local pathology that may cause urinary symptoms (e.g. interstitial cystitis, tumor, bladder stone). Renal insufficiency stade 3 or 4 (creatinine clearance < 35 mL/min) Any allergy or contraindication to ciprofloxacin or drugs used in this protocole (xylocaine, Atarax, paracetamol, and nonsteroidal anti-inflammatory drug) Any allergy to intravenous contrast agent or iodine Thyrotoxicosis Concomitant use of tizanidine Patients participating to another research protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Romain CAREMEL, MD
Organizational Affiliation
Rouen University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rouen University Hospital
City
Rouen
ZIP/Postal Code
76031
Country
France

12. IPD Sharing Statement

Learn more about this trial

Results of Selective Prostatic Arterial Embolization in Patients With Indwelling Urinary Catheter Due to Benign Prostatic Hyperplasia Refractory to Medical Treatment.

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