COMETH study.
- Conditions
- cervical (pre)malignant diseasehigh risk human papillomavirus(voorstadia van) baarmoederhalskankerhoogrisico humaan papillomavirus
- Registration Number
- NL-OMON23076
- Lead Sponsor
- VU University Medical Center
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 300
Inclusion Criteria
1. Women 18-70 years of age;
2. Cervical smear is hr-HPV DNA positive;
Exclusion Criteria
1. Women unable to take a self-sample (including a physical or mental handicap);
2. Cervical smear is hr-HPV DNA negative;
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Endpoint is histology outcome; i.e. presence or absence of ≥CIN2 lesions.
- Secondary Outcome Measures
Name Time Method