Clinical Trial Details

Overview

Research Study Summary

Enlarged Prostate (BPH) Study

Purpose

A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel Group Study of the Efficacy and Safety of Intraprostatic Administration of BOTOX 200 U (Botulinum Toxin Type A) Purified Neurotoxin Complex to Treat Lower Urinary Tract Symptoms due to Benign Prostatic Hyperplasia

Patient Inclusion Criteria:

  • Males 45 years or older weighing at least 110 pounds
  • Lower urinary tract symptoms for at least the last 6 months, currently taking or history of taking approved prostate medications

Patient Exclusion Criteria:

  • Prostatitis, prostate cancer, bladder cancer, previous prostate surgery or bladder surgery
  • Frequent UTI's, symptomatic kidney stones or planned intervention for kidney stones
  • Uninvestigated hematuria, Interstitial Cystitis, neurological disorders
  • Clotting factor deficiencies or platelet disorders, HIV, uncontrolled diabetes
  • Over-active bladder or bladder medications, urinary incontinence or retention, catheter usage

To Learn more

CW ID: 178206
Date Last Changed: July 19, 2013

Clinical Trial Snapshot

Phase
2
Gender
Male
Age
45 and up
Overall Status
Recruiting
Facility Type
N/A

Contact

West Coast Clinical Research
5525 Etiwanda Ave.
Suite 202
Tarzana, CA 91356
Phone: 818-776-0820
Fax: 818-776-1269

View Map

Research Center Information:

West Coast Clinical Research

Volunteer for this Trial

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