UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000035666
Receipt number R000040632
Scientific Title Pharmacokinetics study of food ingredient. SWE-2018-06-HR1002
Date of disclosure of the study information 2019/01/28
Last modified on 2019/07/01 14:31:51

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Basic information

Public title

Pharmacokinetics study of food ingredient.
SWE-2018-06-HR1002

Acronym

Pharmacokinetics study of food ingredient.

Scientific Title

Pharmacokinetics study of food ingredient.
SWE-2018-06-HR1002

Scientific Title:Acronym

Pharmacokinetics study of food ingredient.

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the pharmacokinetics of food ingredient.

Basic objectives2

Pharmacokinetics

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Plasma concentration of food ingredient and the 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

Single ingestion of test food

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

(1)Male and Female whose age are 20 <= years old <65.
(2)Subjects who are able to submit the written informed consents.

Key exclusion criteria

(1)Subjects who are with treatment.
(2)Subjects who are with history of gastrointestinal surgery.
(3)Subjects who are attending other studies or attended other studies within the past 4 weeks.
(4)Subjects who are;
a)With present heart disorder, liver disorder, or kidney disorder,
b)With history of cardiac disorder,
c)With diabetes mellitus, or
d)With allergy to the study foods.
(5)Subjects who are not negative for syphilis, HBs antigen, HCV antibody, HIV antigen/antibody or HTLV-1 antibody test.
(6)Subjects who are deemed to be unsuitable by the investigator.

Target sample size

16


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yoshiko Ono

Organization

SUNTORY WELLNESS LIMITED

Division name

Institute for Health Care Science

Zip code


Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto, Japan

TEL

050-3182-0627

Email

Yoshiko_Toyoda@suntory.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Namino Tomimori

Organization

SUNTORY WELLNESS LIMITED

Division name

Institute for Health Care Science

Zip code


Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto, Japan

TEL

050-3182-0651

Homepage URL


Email

Namino_Sugiura@suntory.co.jp


Sponsor or person

Institute

SUNTORY WELLNESS LIMITED

Institute

Department

Personal name



Funding Source

Organization

SUNTORY WELLNESS LIMITED

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

2019 Year 01 Month 28 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

2018 Year 11 Month 26 Day

Date of IRB

2018 Year 11 Month 26 Day

Anticipated trial start date

2019 Year 01 Month 29 Day

Last follow-up date

2019 Year 02 Month 24 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2019 Year 01 Month 25 Day

Last modified on

2019 Year 07 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000040632


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name