Clinical study confirming the usefulness of cervical cell self-collection in Human Papilloma Virus test

Clinical study confirming the usefulness of cervical cell self-collection in Human Papilloma Virus test - Clinical study confirming the usefulness of cervical cell self-collection in Human Papilloma Virus test

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000040440

Enrollment

250

Registered

2020-05-18

Start date

2020-05-18

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

HPV infection

Interventions

Subjects will self-collect cervical cells using HSP.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1) Women over 20 and under 50 2) Those who can cooperate with cervical cell collection 3) Those who can obtain written consent from the subject

Exclusion criteria

Exclusion criteria: 1) Those who have judged that it is inappropriate for the investigators to collect during menstruation or less than one week after the menstruation 2) Pregnant women 3) Those who have undergone a total hysterectomy 4) In addition, those who the investigators in charge of research judges to be inappropriate

Design outcomes

Primary

Measure	Time frame
Overall conformity ratio in HPV measurement	—

Secondary

Measure	Time frame
Positive conformity ratio in HPV measurement Negative conformity ratio in HPV measurement	—

Countries

Japan

Contacts

Public ContactHiromasa Takahashi

CMIC Co., Ltd. Clinical Operation 3rd Div.

hiromasa-takahashi@cmic.co.jp03-6779-8000

Outcome results

None listed

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