Effectiveness of the handheld digital cervicography camera in women who underwent colposcopy

Phase 2

Recruiting

• Conditions: Abnormal cervical cancer screening who underwent colposcopy; Abnormal cervical cancer screening; colposcopy; handheld cervicography

• Registration Number: TCTR20230907004
• Lead Sponsor: Faculty of Medicine Siriraj Hospital, Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-09-07
• Study Completion: 2024-03-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 450

Inclusion Criteria

1. Age more than or equal 18 years old
2. Abnormal cervical cancer screening needed colposcopy
3. Not pregnant
4. Informed consent

Exclusion Criteria

None

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
effectiveness At the time of intervention sensitivity, specificity, PPV, NPV

Secondary Outcome Measures

Name	Time	Method
CIN2+ pathology At the time of intervention Colposcopic index/score,Prevalence of high-risk HPV infection 2 weeks after intervention HPV-DNA test