Detection Rates of High-risk Human Papilloma Virus in Women with Abnormal Cervical Cytology: A Comparison between Self-collected and Physician-collected Specimens
Phase 1
Completed
- Conditions
- Cervical Intraepithelial NeoplasiaHPV, self sampling, cervical cancer screening, cervical cancer prevention
- Registration Number
- TCTR20220826006
- Lead Sponsor
- Thai Gynecologic Cancer Society
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 500
Inclusion Criteria
age 18 or more
abnormal cytology or hpv hr positive
agree to participate
Exclusion Criteria
pregnancy
history of cervical cancer or hysterectomy
history of radiation therapy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Self sampling HPV at the end of the study HPV testing
- Secondary Outcome Measures
Name Time Method Knowledge and attitude at the end of the study questionnaire interview