UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029569
Receipt number R000032269
Scientific Title Development of biomarkers of macronutrient intake by integrated analysis of metabolome data between human samples and components derived from foods.
Date of disclosure of the study information 2017/10/18
Last modified on 2018/10/17 09:30:56

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Basic information

Public title

Development of biomarkers of macronutrient intake by integrated analysis of metabolome data between human samples and components derived from foods.

Acronym

Development of biomarkers of macronutrient intake by integrated analysis of metabolome data between human samples and components derived from foods

Scientific Title

Development of biomarkers of macronutrient intake by integrated analysis of metabolome data between human samples and components derived from foods.

Scientific Title:Acronym

Development of biomarkers of macronutrient intake by integrated analysis of metabolome data between human samples and components derived from foods

Region

Japan


Condition

Condition

healthy person

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the change of metabolites of blood and urine samples in human after rice or bread meal intake.

Basic objectives2

Others

Basic objectives -Others

metabomics

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

metabolites

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

Food

Interventions/Control_1

rice, bread

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

Male and Female

Key inclusion criteria

healthy person. no commonly used drugs. no abdominal operation history.

Key exclusion criteria

1. current treatment
2. patients with CVD, liver damage, renal impairment, respiratory disease, endocrine disorders, metabolic disturbance
3. chest pain, faint
4. possibility: allergy from test meal
5. Blood donation (<1 month over 200 ml, <
month over 400ml)
6. inadequate enrollment judged from director

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yoshihito Fujita

Organization

Graduate School of Medicine, Kyoto University

Division name

Department of Diabetes, Endocrinology and Nutrition

Zip code


Address

54 Shogoin, Kawahara-cho, Sakyo-ku, Kyoto

TEL

0757513560

Email

yfujita9@kuhp.kyoto-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yoshihito Fujita

Organization

Graduate School of Medicine, Kyoto University

Division name

Department of Diabetes, Endocrinology and Nutrition

Zip code


Address

54 Shogoin, Kawahara-cho, Sakyo-ku, Kyoto

TEL

0757513560

Homepage URL


Email

yfujita9@kuhp.kyoto-u.ac.jp


Sponsor or person

Institute

Kyoto University

Institute

Department

Personal name



Funding Source

Organization

Japan Agency for Medical Research and Development

Organization

Division

Category of Funding Organization

Japanese Governmental office

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

2017 Year 10 Month 18 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

2017 Year 09 Month 28 Day

Date of IRB


Anticipated trial start date

2017 Year 10 Month 23 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

2017 Year 10 Month 16 Day

Last modified on

2018 Year 10 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000032269


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name