Skip to content

Evaluation of diagnostic efficacy of portable artificial intelligence quantitative ultrasound

Evaluation of diagnostic efficacy of portable artificial intelligence quantitative ultrasound

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060004
Enrollment
Unknown
Registered
2022-05-14
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

osteoporosis

Interventions

Gold Standard:Dual Energy X-ray Absorptiometry was used as the gold standard for discrimination. The diagnostic criterion was referred to the WHO recommended standard, and T-value was used (the compar

Sponsors

Sun Yat-sen Memorial Hospital, Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20-80 years; 2. Patients and their families were informed of the study details and signed informed consent forms; 3. A DXA bone mineral density test has been planned.

Exclusion criteria

Exclusion criteria: 1. Patients with serious heart, lung, liver and kidney failure, malignant tumor, poor general state, mental illness and other patients who cannot cooperate with examination; 2. Not suitable for ultrasound examination.

Design outcomes

Primary

MeasureTime frame
Ultrasonic RF signal;DXA value;Effect value;Speed of sound;

Secondary

MeasureTime frame
Osteoporosis self assessment tools in Asia;Fracture risk assessment tool;

Countries

China

Contacts

Public ContactDing Yue

Sun Yat-sen Memorial Hospital, Sun Yat-Sen University

dingyue@mail.sysu.edu.cn+86 13570133707

Outcome results

None listed

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