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Efficiency evaluation of automated visual evaluation system for cervical lesions diagnosing

Efficiency evaluation of automated visual evaluation system for cervical lesions diagnosing

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100046600
Enrollment
Unknown
Registered
2021-05-22
Start date
2021-06-01
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

cervical lesions

Interventions

Gold Standard:Pathological diagnosis
Index test:Automated&#32
visual&#32
evaluation&#32
system

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 59 Years

Inclusion criteria

Inclusion criteria: Participated in cervical screening in the past, with complete data on cases. Data include: age, cervical cytology, HPV, cervical photos, pathological results of POI protocol.

Exclusion criteria

Exclusion criteria: Cases can not be identified by AVE.

Design outcomes

Primary

MeasureTime frame
coincidence rate of high-grade cervicai lesions;SEN, SPE, ACC, AUC of ROC;—

Countries

China

Contacts

Public ContactHou Jun

Peking University Shenzhen Hospital

h.juner@qq.com+86 13510330709

Outcome results

None listed

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