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

Withdrawn before enrolling

Conditions studied: Benign Prostatic Hyperplasia

In brief

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.

Key facts

Study ID

NCT05784558

Run by

NeoTract, Inc.

People needed

0

Starts

2025-01-26

Expected to finish

2026-09-24

Last updated by the study team

2026-03-11

Who can join

Age: 45 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosis of symptomatic BPH

You may not qualify if…

• Prior surgical intervention for treatment of BPH
• Unable or unwilling to give informed consent or unwilling to complete all required questionnaires and follow-up assessments

Where it is running

• Neotract Inc — Pleasanton, California, United States

Full record on ClinicalTrials.gov

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