UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000034949
Receipt number R000039848
Scientific Title A study on the usefulness of self-harvesting of HPV test and Chlamydia test
Date of disclosure of the study information 2018/11/25
Last modified on 2020/01/07 10:50:54

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Basic information

Public title

A study on the usefulness of self-harvesting of HPV test and Chlamydia test

Acronym

A study on the usefulness of self-harvesting of HPV test and Chlamydia test

Scientific Title

A study on the usefulness of self-harvesting of HPV test and Chlamydia test

Scientific Title:Acronym

A study on the usefulness of self-harvesting of HPV test and Chlamydia test

Region

Japan


Condition

Condition

Cervical cancer
Chlamydia infection

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

We conduct HPV (human papilloma virus) examination by autologous cell harvesting to non-consulted persons who do not have cervical cancer screening examinations, and examine the usefulness of HPV self-harvesting compared with the examination by doctors. The purpose of this study is to find a method leading to the early detection of cervical cancer in the absence of improved gynecological examination rate by verifying the usefulness of self-screening for those who have not undergone cervicl cancer screening examination.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Concordance rate of HPV and Chlamydia between self-harvesting and physician harvesting.

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit

65 years-old >=

Gender

Female

Key inclusion criteria

Healthy women between 20 and 65 years old.
People with sexual experiences.
Those who can obtain consent in participating in this research in writing.

Key exclusion criteria

When there is a possibility of pregnancy

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Mihyon
Middle name
Last name Song

Organization

Marunouchi no Mori Ladies Clinic

Division name

Gynecology

Zip code

1006509

Address

Shin Marunouchi Building, 9th Floor, 1-5-1 Marunouchi, Chiyoda-ku, Tokyo

TEL

03-6206-3900

Email

gyne@med.kawasaki-m.ac.jp


Public contact

Name of contact person

1st name Mihyon
Middle name
Last name Song

Organization

Marunouchi no Mori Ladies Clinic

Division name

Gynecology

Zip code

1006509

Address

Shin Marunouchi Building, 9th Floor, 1-5-1 Marunouchi, Chiyoda-ku, Tokyo

TEL

03-6206-3900

Homepage URL


Email

gyne@med.kawasaki-m.ac.jp


Sponsor or person

Institute

Marunouchi no Mori Ladies Clinic

Institute

Department

Personal name



Funding Source

Organization

Marunouchi no Mori Ladies Clinic

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kawasaki Medical University

Address

Matsushima 577 Kurashiki-shi, Okayama prefecture

Tel

086-462-1111

Email

gyne@med.kawasaki-m.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2018 Year 11 Month 25 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2018 Year 11 Month 17 Day

Date of IRB

2019 Year 02 Month 23 Day

Anticipated trial start date

2018 Year 11 Month 25 Day

Last follow-up date

2019 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

non


Management information

Registered date

2018 Year 11 Month 20 Day

Last modified on

2020 Year 01 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000039848


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name