UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000032157
Receipt number R000036687
Scientific Title Detectability of breast lesions in the low-dose computed tomography
Date of disclosure of the study information 2018/04/09
Last modified on 2018/10/09 10:39:28

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Basic information

Public title

Detectability of breast lesions in the low-dose computed tomography

Acronym

Detectability of breast lesions in the low-dose computed tomography

Scientific Title

Detectability of breast lesions in the low-dose computed tomography

Scientific Title:Acronym

Detectability of breast lesions in the low-dose computed tomography

Region

Japan


Condition

Condition

Breast lesions

Classification by specialty

Breast surgery Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To clarify whether breast lesions indicated in breast cancer screening mammography can be detected in low-dose computed tomography images.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Detectability of breast lesions in the low-dose computed tomography

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Implementation and evaluation of one low-dose chest computed tomography after breast cancer screening

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


Not applicable

Age-upper limit


Not applicable

Gender

Female

Key inclusion criteria

Examinees who received breast cancer screening mammography and were diagnosed that a precise examination was necessary.
Examinees who received ultrasonic examination of precision examination.

Key exclusion criteria

Examinees who have already received lung cancer screening on the same day.

Target sample size

300


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Satoshi Takagi

Organization

Hokkaido University

Division name

Faculty of Health Sciences

Zip code


Address

Kita 12, Nishi 5, Kita-ku, Sapporo, Hokkaido, JAPAN

TEL

011-706-2826

Email

talltree@hs.hokudai.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Satoshi Takagi

Organization

Hokkaido University

Division name

Faculty of Health Sciences

Zip code


Address

Kita 12, Nishi 5, Kita-ku, Sapporo, Hokkaido, JAPAN

TEL

011-706-2826

Homepage URL


Email

talltree@hs.hokudai.ac.jp


Sponsor or person

Institute

Hokkaido University

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science
The Hitachi Global Foundation

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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 04 Month 09 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

Terminated

Date of protocol fixation

2018 Year 04 Month 09 Day

Date of IRB


Anticipated trial start date

2018 Year 06 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 04 Month 09 Day

Last modified on

2018 Year 10 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000036687


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name