Exploratory study for concurrent testing of cervical cytology, high-risk HPV and Chlamydia trachomatis from liquid based cytology.

Exploratory study for concurrent testing of cervical cytology, high-risk HPV and Chlamydia trachomatis from liquid based cytology. - Concurrent testing of cervical cytology, high-risk HPV and Chlamydia trachomatis.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000016839

Enrollment

200

Registered

2015-03-25

Start date

2015-03-26

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Cervical cytology, Sexual transmitted Infection

Interventions

None listed

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Woman aged 20 years or older Woman whom underwent a cervical cancer screening Woman whom underwent a sexually transmitted infection screening

Exclusion criteria

Exclusion criteria: Woman who is pregnant Woman who has a risk for taking a specimen Woman who has difficulty to get the informed consent Woman whom the investigator judged as inappropriate as a subject of this study

Design outcomes

Primary

Measure	Time frame
Association between cervical cytology results and Chlamydia trachomatis and association between high-risk HPV and Chlamydia trachomatis.	—

Countries

Japan

Contacts

Public ContactShusaku Tozaka

Nippon Becton Dickinson Company, Ltd Medical Affairs

shusaku_tozaka@bd.com03-6234-5628

Outcome results