UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000041325
Receipt number R000047139
Scientific Title Effects of honey ingestion on arterial function.
Date of disclosure of the study information 2020/08/17
Last modified on 2023/09/05 19:10:28

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Basic information

Public title

Effects of honey ingestion on arterial function.

Acronym

Effects of honey ingestion.

Scientific Title

Effects of honey ingestion on arterial function.

Scientific Title:Acronym

Effects of honey ingestion.

Region

Japan


Condition

Condition

Healthy young adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effects of single honey ingestion on arterial function.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Arterial stiffness (after 30- and 60-min)
Flow-mediated dilation (after 30- and 60-min)

Key secondary outcomes

Glucose (after 30- and 60-min)


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Placebo

Stratification

YES

Dynamic allocation

YES

Institution consideration

Institution is not considered as adjustment factor.

Blocking

YES

Concealment

Pseudo-randomization


Intervention

No. of arms

3

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Food Behavior,custom

Interventions/Control_1

Control-Water ingestion (0.0 g/kg body weight), single ingestion
Cross-over design of three conditions

Interventions/Control_2

Intervention 1-Normal honey ingestion (0.6 g/kg body weight), single ingestion
Cross-over design of three conditions

Interventions/Control_3

Intervention 2-Kirghiz honey ingestion (0.6 g/kg body weight), single ingestion
Cross-over design of three conditions

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

18 years and older men and women, not restricted by a doctor from exercising, not have medication and smoking.

Key exclusion criteria

Have a cardiovascular and cerebrovascular diseases.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Masato
Middle name
Last name Nishiwaki

Organization

Osaka Institute of Technology

Division name

Faculty of Engineering

Zip code

535-8585

Address

5-16-1 Ohmiya, Asahi-ku, Osaka

TEL

06-6954-4391

Email

masato.nishiwaki@oit.ac.jp


Public contact

Name of contact person

1st name Masato
Middle name
Last name Nishiwaki

Organization

Osaka Institute of Technology

Division name

Faculty of Engineering

Zip code

535-8585

Address

5-16-1 Ohmiya, Asahi-ku, Osaka

TEL

06-6954-4391

Homepage URL


Email

masato.nishiwaki@oit.ac.jp


Sponsor or person

Institute

Center for Research Administration & Social Outreach, Osaka Institute of Technology

Institute

Department

Personal name



Funding Source

Organization

Japan Science and Technology Agency

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

The Human Ethics Committee at the Osaka Institute of Technology

Address

5-16-1 Ohmiya, Asahi-ku, Osaka

Tel

06-4300-6883

Email

Kenkyu@josho.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



Other administrative information

Date of disclosure of the study information

2020 Year 08 Month 17 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

14

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

2020 Year 06 Month 22 Day

Date of IRB

2020 Year 07 Month 20 Day

Anticipated trial start date

2020 Year 08 Month 01 Day

Last follow-up date

2020 Year 11 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2020 Year 08 Month 05 Day

Last modified on

2023 Year 09 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000047139


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name