Inspection Device For Cervical Cancer Screening
Not Applicable
- Registration Number
- CTRI/2017/07/009005
- Lead Sponsor
- IIT Bombay
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Women with an intact uterus, ever married, Women patients who visit the hospital for PAP Smear will also be enrolled, with prior consent.
Exclusion Criteria
Women who are pregnant /undergone hysterectomy/ treated for pre-cancers or cancers in the past / menstruating will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Concordance between Gyneacam and Pap smear results.Timepoint: 1 Year
- Secondary Outcome Measures
Name Time Method Quality of imagesTimepoint: 1 year