UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056709
Receipt number R000064822
Scientific Title The construction of AI program which could identify uterine cervical lesion worse than moderate cervical intraepithelial neoplasia
Date of disclosure of the study information 2025/01/14
Last modified on 2025/01/14 13:50:38

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Basic information

Public title

The construction of AI program which could identify uterine cervical lesion worse than moderate cervical intraepithelial neoplasia

Acronym

The construction of AI program which could identify uterine cervical lesion worse than moderate cervical intraepithelial neoplasia

Scientific Title

The construction of AI program which could identify uterine cervical lesion worse than moderate cervical intraepithelial neoplasia

Scientific Title:Acronym

The construction of AI program which could identify uterine cervical lesion worse than moderate cervical intraepithelial neoplasia

Region

Japan


Condition

Condition

uterine cervical intraepithelial neoplasia

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The construction of AI program which could identify uterine cervical lesion worse than moderate cervical intraepithelial neoplasia with images by smartphone

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

The construction of AI program which could identify uterine cervical lesion worse than moderate cervical intraepithelial neoplasia with images by smartphone

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


Not applicable

Gender

Female

Key inclusion criteria

the patients with uterine cervical cellular aberration who need tissue examination

Key exclusion criteria

the patients who had receive treatment for uterine cervix

Target sample size

450


Research contact person

Name of lead principal investigator

1st name Norikatsu
Middle name
Last name Miyoshi

Organization

Osaka University Graduate School of Medicine

Division name

Department of Gastroenterological Surgery

Zip code

5650871

Address

2-2, Yamadaoka Suita, Osaka 567-0871, Japan

TEL

0668793251

Email

nmiyoshi@gesurg.med.osaka-u.ac.jp


Public contact

Name of contact person

1st name Ai
Middle name
Last name Miyoshi

Organization

Kanda Maternity Clinic Annex

Division name

Gynecology

Zip code

5640053

Address

5-26-3F Enokicho Suita, Osaka, Japan

TEL

0663397241

Homepage URL


Email

aimiyoshi20090808@yahoo.co.jp


Sponsor or person

Institute

Others

Institute

Department

Personal name



Funding Source

Organization

None

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

Osaka University Hospital

Address

2-2, Yamadaoka Suita, Osaka 567-0871, Japan

Tel

0662108296

Email

rinri@hp-crc.med.osaka-u.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

2025 Year 01 Month 14 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

Open public recruiting

Date of protocol fixation

2024 Year 02 Month 02 Day

Date of IRB

2024 Year 02 Month 20 Day

Anticipated trial start date

2024 Year 02 Month 27 Day

Last follow-up date

2029 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

We take uterine cervical images by smartphone when we examine of cervix using a lighted magnifying instrument called a colposcopy. We compare images and biopsy results and construct AI program.


Management information

Registered date

2025 Year 01 Month 14 Day

Last modified on

2025 Year 01 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064822