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Role of Artificial Intelligence for detection of pre-cancerous and cancerous cervical lesions

Not Applicable
Registration Number
CTRI/2023/02/049936
Lead Sponsor
Government Medical college and hospital Chandigarh
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Sexually active women above the age of 30 (as recommended by WHO guidelines 2021)

Exclusion Criteria

Type 3 squamocolumnar junction

Active bleeding per vaginum

Frank growth on the cervix

Post hysterectomy

History of treatment of cancerous lesions

Acute cervical infection or pelvic inflammatory disease (patients can be included after treatment)

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the diagnostic accuracy of the Smartscope® for detection of pre-cancerous and cancerous lesions of the cervix using cytology or histopathology as the reference standardTimepoint: At first visit (when smartscope used), on collection of Pap report ,on collection of cervical biopsy report
Secondary Outcome Measures
NameTimeMethod
To compare the Swede score calculated by the observer with the AI-based diagnosis keeping cytology and histopathology as the reference standardTimepoint: At first visit (when smartscope used), on collection of Pap report ,on collection of cervical biopsy report
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