Early detection of cervical neoplasia by visual screening and hybrid capture testing by self and physician collection methodology - A community based study in rural area
Not Applicable
- Registration Number
- CTRI/2010/091/006076
- Lead Sponsor
- Qiagen India Pvt.Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 1000
Inclusion Criteria
Age > 30 years of age
Ability to give informed consent
Sexually active
No debilitating disease (physically able to undergo study procedures)
Exclusion Criteria
Women who have undergone excision biopsy, cryotherapy and conisation and hysterectomy,Acute cervicitis or vaginitis,Pregnancy
Severe debilitating disease.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Detection of CIN via HPV testTimepoint: 1 year
- Secondary Outcome Measures
Name Time Method Comparison of self sampling with physician.<br>comparison of VIA-VILI with HC2.Timepoint: 1 Year