UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000030192
Receipt number R000034488
Scientific Title Examination of the efficacy of ChemoCalc in the explanation of the breast cancer adjuvant treatment
Date of disclosure of the study information 2017/12/01
Last modified on 2020/03/23 12:19:15

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Basic information

Public title

Examination of the efficacy of ChemoCalc in the explanation of the breast cancer adjuvant treatment

Acronym

Examination of the efficacy of ChemoCalc in the explanation of the breast cancer adjuvant treatment

Scientific Title

Examination of the efficacy of ChemoCalc in the explanation of the breast cancer adjuvant treatment

Scientific Title:Acronym

Examination of the efficacy of ChemoCalc in the explanation of the breast cancer adjuvant treatment

Region

Japan


Condition

Condition

breast cancer

Classification by specialty

Breast surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To examine the understanding about drug costs, we conduct a randomized controlled trial using ChemoCalc at explanation of the breast cancer adjuvant treatment .

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

Understanding about drug costs

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Cluster

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

Using software of calculating drug costs

Interventions/Control_2

Disuding software of calculating drug costs

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

Male and Female

Key inclusion criteria

The patients who planned initiation of the adjuvant postoperative treatment

Key exclusion criteria

Patients with dementia

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Susumu
Middle name
Last name Eguchi

Organization

Nagasaki University Graduate School of Biomedical Science

Division name

Surgery

Zip code

8528501

Address

1-17-1, Sakamoto-machi

TEL

095-849-7316

Email

sueguchi@nagasaki-u.ac.jp


Public contact

Name of contact person

1st name Sayaka
Middle name
Last name Kuba

Organization

Nagasaki University Graduate School of Biomedical Science

Division name

Surgery

Zip code

8528501

Address

1-7-1, Sakamoto-machi, Nagasaki city

TEL

095-849-7316

Homepage URL


Email

skuba@nagasaki-u.ac.jp


Sponsor or person

Institute

Nagasaki University Graduate School of Biomedical Science

Institute

Department

Personal name



Funding Source

Organization

none

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

Nagasaki University Hospital review board

Address

1-7-1, Sakamoto-machi, Nagasaki city

Tel

0958192503

Email

gaibushikin@ml.nagasaki-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

2017 Year 12 Month 01 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled

20

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

2017 Year 11 Month 29 Day

Date of IRB

2017 Year 11 Month 29 Day

Anticipated trial start date

2017 Year 12 Month 01 Day

Last follow-up date

2019 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 11 Month 30 Day

Last modified on

2020 Year 03 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034488


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name