UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000037160
Receipt number R000042302
Scientific Title Effects of intake of a test food on postprandial blood triglyceride level -a randomized, double blind placebo-controlled, cross-over study-
Date of disclosure of the study information 2019/07/02
Last modified on 2022/06/30 13:36:23

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Effects of intake of a test food on postprandial blood triglyceride level -a randomized, double blind placebo-controlled, cross-over study-

Acronym

Effects of a test food on postprandial blood triglyceride level

Scientific Title

Effects of intake of a test food on postprandial blood triglyceride level -a randomized, double blind placebo-controlled, cross-over study-

Scientific Title:Acronym

Effects of a test food on postprandial blood triglyceride level

Region

Japan


Condition

Condition

Healthy adult (who has fasting blood triglyceride level less than 150 mg/dl)

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effect of a test food on postprandial blood triglyceride level after intake of high fat diet

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The differences of serum triglyceride level at sequential sampling time point and AUC (area under the blood concentration - time curve)

Key secondary outcomes

The change of serum RLP cholesterol level at sequential sampling time point and AUC

Other lipid metabolism related factors (total cholesterol, LDL-cholesterol, HDL-cholesterol, free fatty acid, lipoprotein (a,b), lipoprotein fraction (HDL, LDL, VLDL), phospholipid)


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Single ingestion of the placebo food - washout period (more than 6 days) - single ingestion of the test food

Interventions/Control_2

Single ingestion of the placebo food - washout period (more than 6 days) - single ingestion of the test food

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) Healthy subjects aged 20 to 64 years old.
(2) Subjects whose fasting serum triglyceride levels are less than 150 mg/dL in medical check up within 1 year
(3) Subjects who gave written informed consent.

Key exclusion criteria

a. Subjects who have a history of treatment for malignancy, heart failure and myocardial infarction
b. Subjects who have been treated for the following chronic diseases: atrial fibrillation, arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes, dyslipidemia, hypertension, etc.
c. Subjects who frequently use oral medication and/or supplements and/or functional foods (include traditional Chinese medicine) could affect lipid metabolism.
d. Subjects who have allergy (medical products, test food related food)
e. Subjects who are planned to get pregnant after informed consent for the current study or are pregnant or breastfeeding.
f. Subjects who are judged as unsuitable for the study by the physician in charge for other reason.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Atsushi
Middle name
Last name Yamatsu

Organization

Pharma Foods International Co., Ltd.

Division name

R&D department

Zip code

615-8245

Address

1-49, Goryo-Ohara, Nishikyo-ku, Kyoto, Japan

TEL

0753948605

Email

a-yamatsu@pharmafoods.co.jp


Public contact

Name of contact person

1st name Hiroaki
Middle name
Last name Yamada

Organization

Pharma Foods International Co., Ltd.

Division name

R&D department

Zip code

615-8245

Address

1-49, Goryo-Ohara, Nishikyo-ku, Kyoto, Japan

TEL

0753948605

Homepage URL


Email

h-yamada@pharmafoods.co.jp


Sponsor or person

Institute

Pharma Foods International Co., Ltd

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

Ethics Committees of Nihonbashi Egawa Clinic

Address

Kotobuki Building.2F, 1-1-3, Yaesu, Chuo-ku, Tokyo, Japan)

Tel

03-5204-0311

Email

jim@medipharma.co.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

2019 Year 07 Month 02 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

30

Results


Results date posted


Results Delayed

Delay expected

Results Delay Reason

delay of data analysis

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

2019 Year 06 Month 14 Day

Date of IRB

2019 Year 06 Month 14 Day

Anticipated trial start date

2019 Year 06 Month 19 Day

Last follow-up date

2020 Year 04 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2023 Year 12 Month 30 Day


Other

Other related information



Management information

Registered date

2019 Year 06 Month 25 Day

Last modified on

2022 Year 06 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000042302


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name