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Clinical Study of an AI-Based Uroflowmetry System

Clinical Study of an AI-Based Uroflowmetry System

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108828
Enrollment
Unknown
Registered
2025-09-08
Start date
2025-09-15
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lower Urinary Tract Dysfunction

Interventions

Gold Standard:Laborie Aquarius TT® Desktop Uroflowmetry Measuring Maximum Urine Flow Rate (Qmax), Average Urine Flow Rate (Qavg), Urine Volume (Uvol), and Urination Time (Utime)
Index test:Maximum urinary flow rate (Qmax), average urinary flow rate (Qavg), urine volume (Uvol), and voiding time (Utime) measured by the AI-UFD Urinary Flow Detection System

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University Yuedong Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Male aged >=18 years; 2.Diagnosed with LUTS/BPH; 3.Able to urinate independently.

Exclusion criteria

Exclusion criteria: 1.Neurogenic bladder, urethral stricture; 2.Acute urinary tract infection; 3.Requiring continuous catheterization or late-stage malignant tumor; 4.Unable to cooperate or data missing.

Design outcomes

Primary

MeasureTime frame
Peak urinary flow rate;Voided volume;Average urinary flow rate;

Secondary

MeasureTime frame
Voiding time;IPSS Score;Patient compliance;

Countries

China

Contacts

Public ContactWang Yu

The Third Affiliated Hospital of Sun Yat-sen University Yue Dong Hospital

wangyu79@mail.sysu.edu.cn+86 139 2957 1713

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026