Investigating Medication vs. Prostatic Urethral Lift: Assessment and Comparison of Therapies for Benign Prostatic Hyperplasia

Status: Recruiting
Location: See location...
Intervention Type: Drug, Device
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This prospective, multicenter, two-arm, 1:1 randomized controlled trial (RCT) will enroll approximately 250 males at approximately 25 sites located within the United States. All enrolled subjects will be 45 years of age or older diagnosed with symptomatic benign prostatic hyperplasia (BPH). They will be randomized to one of two readily available, marketed BPH therapies; Prostatic Urethral Lift procedure with the UroLift System (PUL Arm) or 0.4mg tamsulosin HCl (MED Arm).

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 45
Healthy Volunteers: t
View:

• Male 45 years of age or older

• Diagnosis of BPH

• Experiencing symptoms of BPH as indicated by an IPSS ≥8 and ≤30

• Willing to wash out of current BPH medication(s), as applicable

• An appropriate candidate for both BPH therapies evaluated in this study.

• Ability to understand and consent to participate in this study

• Willing and able to participate in follow-up evaluations

Locations
United States
California
Neotract
RECRUITING
Pleasanton
Contact Information
Primary
Rogers Mitchell
rogers.mitchell@neotract.com
805-403-7107
Time Frame
Start Date: 2021-12-06
Estimated Completion Date: 2025-10
Participants
Target number of participants: 250
Treatments
Active_comparator: Prostatic Lift
Treatment with the UroLift System
Active_comparator: Medication
Treatment with Tamsulosin HCl 0.4mg
Related Therapeutic Areas
Sponsors
Leads: NeoTract, Inc.

This content was sourced from clinicaltrials.gov