Cancer testing
Phase 4
- Conditions
- Health Condition 1: null- Cervical Screening
- Registration Number
- CTRI/2017/08/009335
- Lead Sponsor
- Mobile Optical Detection Technologies
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subject is able to read, understand and sign the informed consent form
Exclusion Criteria
Subjects with documented dementia or any other mental disorders, which would render them unable to cooperate with the study requirements
Not willing to sign Informed Consent Form
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Increase of negative predictive value (NPV) of the primary screening test to reduce unnecessary referrals to colposcopy and increase of positive predictive value (PPV) in the primary screening test around staging of pre-cancer and cancer, to ensure that women who are at risk for cervical cancer are caught in time for treatmentTimepoint: day 1
- Secondary Outcome Measures
Name Time Method ilTimepoint: Nil