UroLift System TOlerability and ReCovery When Administering Local Anesthesia

NACompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

April 30, 2013

Primary Completion Date

October 31, 2014

Study Completion Date

September 4, 2018

Conditions
Benign Prostatic Hyperplasia
Interventions
DEVICE

UroLift® System

The NeoTract UroLift System is a medical device approved for sale in the European Union, Australia, and Canada. The UroLift® System is indicated for the treatment of symptoms due to urinary outflow obstruction secondary to benign prostatic hyperplasia (BPH) in men 50 years of age or older. During the procedure, an implant is delivered into the prostatic lobe obstructing the urethra and restricting urine flow. The distal end of the device is used to compress the lobe then the implant is delivered to retain the lobe in position, thereby increasing the urethral opening and reducing the fluid obstruction through the prostatic urethra.

Trial Locations (7)

21237

Chesapeake Urology, Baltimore

29572

Carolina Urologic Research Center, Myrtle Beach

32114

Advanced Urology Institute, Daytona Beach

33710

Pinellas Urology, St. Petersburg

84124

Jean Brown Research, Salt Lake City

89144

Sheldon J. Freedman, M.D., Ltd., Las Vegas

92123

Genesis Research LLC, San Diego

All Listed Sponsors
lead

NeoTract, Inc.

INDUSTRY

NCT01876706 - UroLift System TOlerability and ReCovery When Administering Local Anesthesia | Biotech Hunter | Biotech Hunter