Screening methods of cervical cancer- A comparative analysis
Not Applicable
Completed
- Conditions
- Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
- Registration Number
- CTRI/2020/08/027023
- Lead Sponsor
- Gajra Raja Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 500
Inclusion Criteria
All sexually active women and women in reproductive age group with recurrent episodes of white discharge, postcoital bleeding and intermenstrual bleeding.
Exclusion Criteria
Women who refused to give consent and known cases of cervical carcinoma, pregnant women, women with active vaginal bleeding
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method For women who are devoid of any screening test, VIA based screenng will be a good screening tool.Timepoint: At the end of the study (i.e, 1 year)
- Secondary Outcome Measures
Name Time Method To calculate the sensitivity and specificity of VIA screeing of carcinoma cervix.Timepoint: At the end of the study (i.e, 1 year)