Last updated on February 2018

Post-Marketing Study Using PROLIEVE for the Treatment of Benign Prostatic Hyperplasia (BPH)


Brief description of study

The primary objective of the post-marketing study is to collect safety and effectiveness data for 5 years on subjects treated with Prolieve. The collection of 5-year safety information will be used to evaluate the occurrence of any long-term side effects from the treatment. The collection of long-term effectiveness data on subjects treated with Prolieve will provide information on the long-term effects of treatment and time to re- treatment (any treatment initiated for BPH since Prolieve'" treatment, including a second treatment with Prolieve").

Clinical Study Identifier: NCT02021032

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Winter Park Urology

Orlando, FL United States
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Midtown Urologic Trials, PC

New York, NY United States
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North Fulton Urology

Roswell, GA United States
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Mobley Research Center

Houston, TX United States
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Merrimack Urology Associates PC

Chelmsford, MA United States
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Regional Urology

Shreveport, LA United States
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Recruitment Status: Open


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