Feasiblity of Self-Obtained VAginal Sample for Detection of HPV DNA

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004283

Enrollment

151

Registered

2019-09-06

Start date

2019-09-30

Completion date

Unknown

Last updated

2020-04-21

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

Conditions

None listed

Interventions

Medical Device : To investigate any difference of detection rate of HPV DNA in self-obtained vaginal sample using G+KIt(R) and phsician obtained cervical sample.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: •20~65 year aged women with previous sexuall contact and history of HPV positive or abnormal cytology of ASCUS(Atypical squamous cells of undetermined significance) or more

Exclusion criteria

Exclusion criteria: •Woman without sexuall contact •Woman with mentruation and any disease which limits the sampling •Woman who cannot read and understand the guideline •When the physician determined that she is not able to perfome the study

Design outcomes

Primary

Measure	Time frame
Differnce of HPV positivity between the vaginal and cevical samples	—

Secondary

Measure	Time frame
Feasibility of self sampling	—

Countries

Korea, Republic of

Contacts

Public ContactDongryung Shin

Korea Cancer Center Hospital

Outcome results