Evaluation of the Aulea Veloxion™ Disposable Resectoscope System for Operational Efficiency in Surgical Management of Benign Prostatic Hyperplasia (BPH)
Starting soon · Not applicable
Conditions studied: BPH (Benign Prostatic Hyperplasia)
In brief
Prospective, single-arm, single-site, post-market device study; all procedures use Veloxion™ per IFU.
Key facts
- Study ID
- NCT07728071
- Run by
- Chinese University of Hong Kong
- People needed
- 20
- Starts
- 2026-07-16
- Expected to finish
- 2027-12-31
- Last updated by the study team
- 2026-08-03
Who can join
Age: 30 and older, up to 70. Sex: male. Healthy volunteers: not accepted.
You may qualify if…
- Age 30-70 years old with symptomatic BPH.
- Prostate volume 20-120 mL (TRUS/MRI/US)
- Suitable for endoscopic resection/vaporization per device IFU.
- Able to consent and comply with follow-up to 1 month.
You may not qualify if…
- Known/suspected prostate cancer requiring oncologic management.
- Prior prostate surgery impacting urethral anatomy within 12 months.
- Prior implant affecting urethral anatomy.
- Active UTI or untreated bacteriuria pre-op.
- Uncorrectable coagulopathy; inability to manage antithrombotics.
- Severe medical comorbidity precluding anesthesia or endoscopy.
Where it is running
- Prince of Wales Hospital — Shatin, Hong Kong
Full record on ClinicalTrials.gov
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