NCT05784558

RELIEF Study: Real-world Evaluation of LUTS Interventions and Patient Experience During Follow-up

• Status: Withdrawn
• Phase: —
• Study type: Observational
• Enrollment: 0 (actual)
• Sponsor: NeoTract, Inc. · Industry
• Sex: Male
• Age: 45 Years
• Healthy volunteers: Not accepted

Summary

The objective of the RELIEF Study is to compare the safety, effectiveness and patient experience outcomes in real-world subjects treated with different modalities for symptomatic BPH.

Conditions

• Benign Prostatic Hyperplasia

Interventions

Type	Name	Description
DEVICE	UroLift System	The UroLift System is a procedure that utilizes tiny implants to lift and hold the enlarged prostate tissue out of the way so it no longer blocks the urethra.
OTHER	Watchful Waiting or BPH Medications	Subjects for whom the physician decides the best course of therapy to be either watchful waiting or new or continuing BPH medications.
DEVICE	Other Surgical Intervention	Physician decides the best course of therapy to be a surgical intervention other than the UroLift System.

Timeline

• Start date: 2025-01-26
• Primary completion: 2026-01-26
• Completion: 2026-09-24
• First posted: 2023-03-27
• Last updated: 2026-03-11

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study