UMIN-CTR Clinical Trial

Recruitment status Preinitiation
Unique ID issued by UMIN UMIN000046680
Receipt No. R000053250
Scientific Title The acute effect of plant extract residues on postprandial blood triglyceride
Date of disclosure of the study information 2023/02/20
Last modified on 2022/01/20 (Ver. 4)

* 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 Postprandial blood lipid trial
Acronym Postprandial blood lipid trial
Scientific Title The acute effect of plant extract residues on postprandial blood triglyceride
Scientific Title:Acronym Postprandial blood lipid trial
Region
Japan

Condition
Condition Healthy adults
Classification by specialty
Adult
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To investigate the postprandial blood lipids in plant extract residues intake.
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Postprandial blood triglycerides
Key secondary outcomes

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 Plant extract residue 300mg / time
Interventions/Control_2 Placebo food 300mg / time
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
60 years-old >
Gender Male and Female
Key inclusion criteria Persons who is generally judged as healthy
Key exclusion criteria (1) Persons who have any dietary supplements, quasi drugs or medicines which cause same or similar efficacy with the effect evaluated in this study

(2) Persons who have changed their habitats to take supplements or

to use cosmetics within past 4 weeks.

(3) Persons who work in night shift or in day and night shift

(4) Persons who have been treated their illness or prevention in a clinic at their informed consent

(5) Persons with their medical histories as follows: serious diseases of sugar metabolism, lipid metabolism, hepatic function, renal function, heart, circulatory, respiratory, endocrine system, immune system, or mental illness of the nervous system

(6) Persons with the medical histories of alcoholism or drug dependence

(7) Persons who might be developed allergic reaction to foods.

(8) Persons who are pregnant, breast-feeding, or hope to be pregnant during the study period

(9) Persons who had always participated in or will participate in any other clinical trial (to use foods/medicine/quasi medicine/medical device)

(10) Persons who will not be judged suitable to the participants by the investigator.
Target sample size 15

Research contact person
Name of lead principal investigator
1st name Koichiro
Middle name
Last name Ohnuki
Organization Kindai University
Division name Faculty of humanity-oriented science and engineering
Zip code 820-0011
Address 11-6, Kayanomori, Iizuka-shi, Fukuoka
TEL 0948-22-5655
Email ohnuki@fuk.kindai.ac.jp

Public contact
Name of contact person
1st name Koichiro
Middle name
Last name Ohnuki
Organization Kindai University
Division name Faculty of humanity-oriented science and engineering
Zip code 820-0011
Address 11-6, Kayanomori, Iizuka-shi, Fukuoka
TEL 0948-22-5655
Homepage URL
Email ohnuki@fuk.kindai.ac.jp

Sponsor
Institute Faculty of humanity-oriented science and engineering ,Kindai University
Institute
Department

Funding Source
Organization Toyotama Healthy Food Co., Ltd.
Organization
Division
Category of Funding Organization Profit organization
Nationality of Funding Organization

Other related organizations
Co-sponsor Faculty of Agriculture, Kyushu University
Name of secondary funder(s)

IRB Contact (For public release)
Organization Kindai University Faculty of Industrial Science and Technology Ethics Committee
Address 11-6, Kayanomori, Iizuka-shi, Fukuoka
Tel 0948-22-5655
Email ohnuki@fuk.kindai.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 九州大学農学研究院 環境農学部門 森林圏環境資源科学研究室


Other administrative information
Date of disclosure of the study information
2023 Year 02 Month 20 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 Preinitiation
Date of protocol fixation
2022 Year 01 Month 17 Day
Date of IRB
Anticipated trial start date
2022 Year 02 Month 12 Day
Last follow-up date
2022 Year 02 Month 20 Day
Date of closure to data entry
2022 Year 03 Month 06 Day
Date trial data considered complete
2022 Year 03 Month 20 Day
Date analysis concluded
2022 Year 04 Month 20 Day

Other
Other related information

Management information
Registered date
2022 Year 01 Month 20 Day
Last modified on
2022 Year 01 Month 20 Day


Link to view the page
URL(English) https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053250