Study of Median Lobe Prostatic UroLift Procedure



Status:Recruiting
Conditions:Hematology, Urology
Therapuetic Areas:Hematology, Nephrology / Urology
Healthy:No
Age Range:50 - Any
Updated:6/9/2016
Start Date:February 2016
End Date:February 2018
Contact:Emily A Hergenreter
Email:ehergenreter@neotract.com
Phone:6507395570

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The purpose of this study is to evaluate the safety and effectiveness of using UroLift in
subjects with a prostatic median lobe enlargement due to BPH.

Study Objectives: Evaluate the safety and effectiveness of the UroLift® System when used in
symptomatic benign prostatic hyperplasia (BPH) subjects with an enlarged median lobe.

Study Design: Prospective, multicenter, non-blinded, single arm (non-randomized) study.

Sample Size: A total of no more than 40 subjects will be enrolled. Subject Population: Males
age of 50 years or older diagnosed with lower urinary tract symptoms (LUTS) with enlarged
median lobe.

Inclusion Criteria:

- Enlarged median lobe (ML) contributing to obstruction of the prostate

- BPH

Exclusion Criteria:
We found this trial at
7
sites
Omaha, Nebraska 68114
Principal Investigator: Euclid R. deSouza, MD
Phone: 402-399-7892
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Omaha, NE
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Baltimore, Maryland 21237
Principal Investigator: Ron Tutrone, MD
Phone: 443-471-5829
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Baltimore, MD
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Edmonds, Washington 98026
Principal Investigator: Douglas H. Grier, MD
Phone: 425-775-7166
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Edmonds, WA
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San Diego, California 92134
Principal Investigator: Sean P Stroup, MD
Phone: 619-532-7200
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San Diego, CA
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Sherman Oaks, California 91411
Principal Investigator: Richard David, MD
Phone: 818-990-5020
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Sherman Oaks, CA
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Virginia Beach, Virginia 23462
Principal Investigator: Gregg R. Eure, MD
Phone: 757-452-3461
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Virginia Beach, VA
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Winston Salem, North Carolina 27157
Principal Investigator: Dan Rukstalis, MD
Phone: 336-716-1352
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Winston Salem, NC
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