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Clinical Trials in the UK / NCT04338776
Active, not recruiting Not applicable

Comparing UroLift Experience Against Rezūm

NCT04338776 · tracked via the Priya Life Science UK tracker
Sponsor
NeoTract, Inc.
Phase
Not applicable
Started
2021-01-22
Last updated
2025-10-14

Condition(s) studied

Benign Prostatic Hyperplasia

Investigational drug(s) / intervention(s)

UroLiftRezum

UroLift: The UroLift System is indicated for the treatment of symptoms due to urinary outflow obstruction secondary to benign prostatic hyperplasia (BPH). 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.

Rezum: The Rezūm™ System is intended to relieve symptoms, obstructions, and reduce prostate tissue associated with BPH. The Rezūm System is manufactured by Boston Scientific and consists of a radiofrequency (RF) generator and a single-use transurethral delivery device. The Rezūm System utilizes radiofrequency current to generate "wet" thermal energy in the form of water vapor, which is then injected into the transition zone and/or median lobe of the prostate tissue in controlled 9-second doses. The vapor that is injected into the prostate tissue rapidly disperses through the interstitial space between the tissue cells. As the vapor cools, it condenses immediately on contact with tissue and the stored thermal energy is released,reducing the volume tissue adjacent to the urethra.

Study summary

C.L.E.A.R. Study is poised to compare the patient experience post procedure, including catheterization needs as well as retreatment and BPH medication rates following treatment with either the UroLift® System or Rezūm™ System through 12 months.

Eligibility

Sex
MALE
Min age
50 Years
Max age
Healthy volunteers
Accepted
Inclusion Criteria: 1. Male gender 2. Age ≥ 50 years 3. Diagnosis of symptomatic BPH 4. Prostate volume 30cm3 ≤ 80cm3 5. Willing to sign study informed consent form Exclusion Criteria: 1. Current urinary tract infection 2. Current catheter dependent urinary retention or PVR \>= 500 mL 3. Urethra conditions that may prevent insertion of delivery system into bladder 4. Previous BPH surgical procedure 5. Urinary incontinence presumed due to incompetent sphincter 6. Current gross hematuria 7. Patients with a urinary sphincter implant 8. Patients who have a penile prosthesis 9. Currently enrolled in any other investigational clinical research trial that has not completed the primary endpoint

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Tower Urology Los Angeles California
Comprehensive Urology Royal Oak Michigan
NYU Winthrop Urology Garden City New York
Weil Cornell Medical College, Cornell University New York New York
Urology Austin Austin Texas
UT Southwestern Medical Center Dallas Texas
Urology San Antonio San Antonio Texas
Frimley Park Hospital Frimley Camberley
NORFOLK and Norwich University Hospital Norwich Norfolk
Cambridge University Hospitals NHS Foundation Trust Cambridge United Kingdom
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04338776 on ClinicalTrials.gov ↗ ← All trials in the UK