search
Back to results

Prophylactic Vs. Therapeutic Use of Uroxatrol in Men Undergoing Brachytherapy

Primary Purpose

Prostate Cancer

Status
Unknown status
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Uroxatrol (drug)
Sponsored by
New York Prostate Institute
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Prostate, cancer, Brachytherapy, Alpha Blocker

Eligibility Criteria

0 Years - undefined (Child, Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria: 1) Informed consent must be obtained. 2) Men of any age 3) Diagnosis of prostate cancer that is clinically localized 4) Patients must be eligible for permanent prostate brachytherapy either alone or with combination of other treatments (i.e. External beam radiation or hormonal therapy) Exclusion Criteria: Refusal to participate in the study Prior use of alpha-blocker or anti-cholinergic medication in the treatment of prostate hypertrophy. Contraindication to using an alpha-blocker

Sites / Locations

  • New York Prostate Institute

Outcomes

Primary Outcome Measures

IPSS and sexual function QOL life

Secondary Outcome Measures

Safety and tolerance

Full Information

First Posted
September 12, 2005
Last Updated
September 12, 2005
Sponsor
New York Prostate Institute
Collaborators
Sanofi
search

1. Study Identification

Unique Protocol Identification Number
NCT00201630
Brief Title
Prophylactic Vs. Therapeutic Use of Uroxatrol in Men Undergoing Brachytherapy
Official Title
Randomized, Open-Labeled Study of Prophylactic Vs. Therapeutic Use of Uroxatrol to Determine Improvements in Urinary Morbidity Following Men Undergoing Prostate Brachytherapy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2005
Overall Recruitment Status
Unknown status
Study Start Date
September 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
New York Prostate Institute
Collaborators
Sanofi

4. Oversight

5. Study Description

Brief Summary
To asess the efficacy of Uroxatrol, an alpha blocker in men undergoing prostate brachytherapy to treat prostate cancer, and whether the use of Uroxatrol in advance of the brachytherapy is better or not than starting it on the day of surgery.
Detailed Description
Prostate brachytherapy is an increasingly popular method of treating clinically localized prostate cancer. The major morbidity of this procedure is obstructive and irritative voiding symptoms. The risk of urinary retention in published series is 10-15%. Voiding symptoms persist up to 1 year following this procedure. The primary experience in treating obstructive and irritative voiding symptoms is in men with benign prostatic hyperplasia (BPH). In patients with moderate to severe voiding symptomatology, based in the American Urological Association (AUA) Symptom Score Index, medical treatment with alpha antagonists has become commonplace. The use of alpha antagonists is based upon the reduction of smooth muscle tone in both the prostate gland and urinary bladder neck by inhibition of alpha1 adrenoceptor, resulting in relaxation of bladder outlet obstruction and increased urinary flow. Alfuzosin hydrochloride was approved by the FDA for treatment of the signs and symptoms of BPH in 2003. Alfuzosin differs from other  1-adrenergic receptor blockers by the absences of a piperidine moiety and the presence of a diaminopropyl spacer, which confers alfuzosin with specific biochemical properties. Affinity studies on human-cloned  1 receptor subtypes show that alfuzosin, like terazosin and doxazosin, is devoid of significant receptor subtype selectivity. In isolated human tissues, however, alfuzosin displays the highest selectivity ratio for the prostate over the vascular tissue (ratio, 544) compared with tamsulosin (90), doxazosin (51), and terazosin (19). Prostate cancer is the most common malignancy in men. One of the most common treatments of prostate cancer is prostate brachytherapy, or radioactive seed implantation. All patients are affected by obstructive and irritative voiding symptoms to various degrees following this procedure due to edema and inflammation induced by trauma and radiation. Many physicians routinely treat obstructive and irritative voiding symptoms following prostate brachytherapy with alpha-blockers. Patients presenting with clinically localized prostate cancer may elect permanent prostate brachytherapy as definitive therapy. The efficacy of such therapy matches that of radical prostatectomy or external beam radiation. Many patients select brachytherapy since it is a single treatment session that is considered minor surgery. Most patients are discharged the same day and they may resume their normal physical activities without restriction almost immediately. However, the trauma of the needle sticks through the perineum coupled with the effects of the radiation can cause a prostatitis with symptoms similar to irritable bladder or benign prostatic hypertrophy. These symptoms can have considerable impact on the quality of life of the patient and many are medicated with alpha-blockers. Several studies have attempted to define how best to predict for and treat these symptoms. However, the incidence and severity of these symptoms is difficult to predict. The prophylactic use of alpha-blockers may better control these symptoms in some men undergoing prostate brachytherapy. The aim of this study is to compare outcomes of urinary morbidity following prostate brachytherapy between patients treated with alfuzosin prior to implantation and patients treated following implantation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate, cancer, Brachytherapy, Alpha Blocker

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Uroxatrol (drug)
Primary Outcome Measure Information:
Title
IPSS and sexual function QOL life
Secondary Outcome Measure Information:
Title
Safety and tolerance

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
0 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 1) Informed consent must be obtained. 2) Men of any age 3) Diagnosis of prostate cancer that is clinically localized 4) Patients must be eligible for permanent prostate brachytherapy either alone or with combination of other treatments (i.e. External beam radiation or hormonal therapy) Exclusion Criteria: Refusal to participate in the study Prior use of alpha-blocker or anti-cholinergic medication in the treatment of prostate hypertrophy. Contraindication to using an alpha-blocker
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Louis Potters, MD
Phone
516-632-3370
Email
pottersl@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Betsy Guzman
Phone
516-632-3370
Email
bguzman@snch.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louis Potters, MD
Organizational Affiliation
New York Prostate Institue
Official's Role
Study Chair
Facility Information:
Facility Name
New York Prostate Institute
City
Oceanside
State/Province
New York
ZIP/Postal Code
11572
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Betsy Guzman
Phone
516-632-3370
Email
bguzman@snch.org
First Name & Middle Initial & Last Name & Degree
Louis Potters, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
8104650
Citation
Lefevre-Borg F, O'Connor SE, Schoemaker H, Hicks PE, Lechaire J, Gautier E, Pierre F, Pimoule C, Manoury P, Langer SZ. Alfuzosin, a selective alpha 1-adrenoceptor antagonist in the lower urinary tract. Br J Pharmacol. 1993 Aug;109(4):1282-9. doi: 10.1111/j.1476-5381.1993.tb13762.x.
Results Reference
background
Links:
URL
http://www.nyprostate.org
Description
New York Prostate Institute web site

Learn more about this trial

Prophylactic Vs. Therapeutic Use of Uroxatrol in Men Undergoing Brachytherapy

We'll reach out to this number within 24 hrs