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

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

TCTR

Registry ID

TCTR20230907004

Enrollment

450

Registered

2023-09-07

Start date

2023-09-11

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abnormal cervical cancer screening who underwent colposcopy Abnormal cervical cancer screening colposcopy handheld cervicography

Interventions

Use of handheld digital cervicography camera together with conventional colposcopy to get the pictures of cervix in women underwent colposcopy

Experimental Device

Handheld digital cervicography camera

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

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

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
effectiveness At the time of intervention sensitivity, specificity, PPV, NPV	—

Secondary

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

Countries

Thailand

Contacts

Public ContactMethawee Ularnwong

Faculty of Medicine Siriraj Hospital, Mahidol University

yoong.mtw@gmail.com0890781973

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026