Clinical Trial

Vivifi Device Safety Evaluation for the Treatment of Benign Prostatic Hyperplasia

Study acronym: BPH
Not Yet Recruiting
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Summary
The study objective is to evaluate the safety and feasibility of the Vivifi device to treat symptomatic, benign prostatic hyperplasia (BPH).
Trial Details
NCT Number NCT07745621
Lead Sponsor Vivifi Medical
Collaborators: RQM Plus
Conditions Benign Prostatic Hyperplasia
Enrollment 20 participants
Start Date 2026-09
Primary Completion 2027-02 (estimated)
Study Completion 2028-12 (estimated)
Updated on ClinicalTrials.gov 2026-08-04