UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000002462
Receipt number R000002765
Scientific Title Evaluation of usefullness of 1H MR spectroscopy for diagnosis of breast tumors.
Date of disclosure of the study information 2009/09/09
Last modified on 2014/09/07 09:26:59

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Basic information

Public title

Evaluation of usefullness of 1H MR spectroscopy for diagnosis of breast tumors.

Acronym

Usefullness of 1H MR spectroscopy of breast tumors

Scientific Title

Evaluation of usefullness of 1H MR spectroscopy for diagnosis of breast tumors.

Scientific Title:Acronym

Usefullness of 1H MR spectroscopy of breast tumors

Region

Japan


Condition

Condition

breast tumor

Classification by specialty

Breast surgery Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate usefullness of 1H MR spectroscopy as malignancy marker of breast tumors

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Measurement of density of choline compounds and tumor size before treatment

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

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

We will perform 1H MR spectroscopy to the patients of the breast cancer and measure the density of choline compounds which related to the composition and metabolism of the phospholipid of cell membrane. In addition, we will use the density of choline compounds as a marker for differential diagnosis of the breast cancer from benign tumors; phylodes tumor, papilloma and fibrocystic disease.

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

1) The patient who is doubted having breast tumor in palpation, sonography, or mammography.
2) The patient who is seen a solid breast tumor more than 1.5cm in minor axis by post-contrasted MRI
3) The patient who signed a written informed consent form.

Key exclusion criteria

1) The patient who has any contraindication on MRI
2) The patient who cannot be taken contrast material of MRI.
3) The patient who has been taken biopsy of the breast tumor
4) The patient who ever has been taken surgery, chemotherapy, radiation or any other therapy for the breast tumor.

Target sample size

140


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Waka Mizukoshi

Organization

International medical center, Saitama medical university

Division name

Diagnostic Radiology

Zip code


Address

Yamane1397-1,Hidaka city, Saitama prefecture

TEL

042-984-4520

Email

wsaito@saitama-med.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Waka Mizukoshi

Organization

International medical center, Saitama medical university

Division name

Diagnostic Radiology

Zip code


Address

Yamane1397-1, Hidaka city, Saitama

TEL

042-984-4520

Homepage URL


Email

wsaito@saitama-med.ac.jp


Sponsor or person

Institute

International medical center, Saitama medical university

Institute

Department

Personal name



Funding Source

Organization

International medical center, Saitama medical university

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


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

2009 Year 09 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

Completed

Date of protocol fixation

2009 Year 10 Month 01 Day

Date of IRB


Anticipated trial start date

2009 Year 10 Month 01 Day

Last follow-up date

2011 Year 09 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2009 Year 09 Month 07 Day

Last modified on

2014 Year 09 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000002765


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name