Development of novel cytologic sampling device for cervical cancer screening

Development of novel cytologic sampling device for cervical cancer screening - Development of novel cytologic sampling device for cervical cancer screening

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000031303

Enrollment

140

Registered

2018-02-14

Start date

2018-04-01

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 cancer and cervical precursor lesion

Interventions

Existing device(Cervex)/Existing device(Cervex) New device/Existing device(Cervex) New device/Existing device(cotton swab) New device/Existing device(YUINO BRUSH)

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Patients aged 20 years or older, patients scheduled to undergo cervical cytology diagnosis, patients who obtained their consent by written document

Exclusion criteria

Exclusion criteria: Patients who doctor judged inappropriate for participation in this study

Design outcomes

Primary

Measure	Time frame
Adverse event at cell collection and measurement the amount of collected cells	—

Secondary

Measure	Time frame
Evaluate appropriateness of specimens and symptoms such as bleeding and pain	—

Countries

Japan

Contacts

Public ContactToshiaki Shibata

Hamamatsu University School of Medicine Obstetrics and gynecology

tshibata@hama-med.ac.jp053-435-2309

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026