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View Clinical Trial (Medical Research Study)
Uroxatral in Men With Benign Prostate Hypertrophy (BPH) and Erectile Dysfunction (ED) - NCT00256399-44106 (Clinical Trial 133263)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy133263.aspx
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City:
Cleveland
State:
OH
Zip Code:
44106
Conditions:
BPH - Erectile Dysfunction
Purpose:
Uroxatral (alfuzosin) may not only help BPH symptoms but may also improve sexual function in males with BPH and ED.
Study summary:
The study will consist of a 30 day screening/washout phase at the end of which qualified subjects will be assigned to alfuzosin 10 mg tablets once a day. Subjects will be treated for 90 days. The total duration of the study will be 120 days.
Criteria:
Inclusion Criteria: - Males 45-75 years of age - Confirmed diagnosis of BPH/lower urinary tract symptoms (LUTS) and ED - Men with steady partner and who agree to attempt sex once a week. Exclusion Criteria: - Prostate cancer - Prostatitis - Penile disease - Cardiac co-morbidity - Pre-existing co-morbid conditions - History of sensitivity to the drug or similar drugs - Enrollment in another clinical trial - Impaired hepatic function - Impaired renal function - Mental conditions rendering subject unable to understand the study - Subjects not likely to comply with protocol
Study is available at:
University Hospitals of Cleveland
Cleveland, OH 44106
United States
Primary Contact:
Ann M Serenko, MS, RN
Email:
ann.serenko@uhhs.com
Phone:
216-844-3515
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit
ClinicalTrials.gov
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Data Source:
ClinicalTrials.gov
Date Processed:
March 15, 2010
Modifications to
this listing:
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Clinical trials are medical research studies designed to test the safety and/or effectiveness of new drugs, devices, or treatments in humans. These studies are conducted worldwide for a range of conditions and illnesses. Learn more about clinical research and participating in a study at
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