UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000048508
Receipt number R000055280
Scientific Title Safety confirmation studies of excessive intake of black vinegar and black ginger extract processed food in healthy adult men and women.
Date of disclosure of the study information 2022/10/01
Last modified on 2023/01/27 09:05:49

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Basic information

Public title

Safety evaluation

Acronym

Safety evaluation

Scientific Title

Safety confirmation studies of excessive intake of black vinegar and black ginger extract processed food in healthy adult men and women.

Scientific Title:Acronym

Safety confirmation studies of excessive intake of black vinegar and black ginger extract processed food in healthy adult men and women.

Region

Japan


Condition

Condition

Healthy adult

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the safety of excessive intake of black vinegar and black ginger extract processed food 5 times as much as the recommended daily intake for 4 weeks.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Laboratory data (Hematologic test, Blood biochemistry test, Urine analysis), Physical examination (Blood pressure/pulsation, Weight/body mass index) and Adverse event
Evaluate at points of 2 weeks and 4 weeks of intake

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

Oral intake 10 tablets of the test product daily for 4 weeks

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

64 years-old >=

Gender

Male and Female

Key inclusion criteria

Healthy adult men and women between the ages of 20 and 64

Key exclusion criteria

(1) Subjects who intake health food richly containing black vinegar and black ginger
(2) Subjects who are judged as unsuitable for this study by the principal investigator based on the results of clinical examination or cardiopulmonary abnormality
(3) Subjects who have possibilities for emerging allergy related to the study
(4) Subjects having a disease requiring regular medication or a history of serious
(5) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination
(6) Subjects who are engaged in day / night shift work, midnight work, or irregular life habits
(7) Subjects who have participated in other clinical studies
(8) Subjects who intend to become pregnant or lactating
(9) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire
(10) Subjects who are judged as unsuitable for the study by the investigator for other reasons

Target sample size

11


Research contact person

Name of lead principal investigator

1st name Jiro
Middle name
Last name Saito

Organization

Medical Station Clinic

Division name

None

Zip code

152-0004

Address

3-12-8, Takaban, Meguro-ku, Tokyo, Japan

TEL

03-6452-2712

Email

info@med-station.jp


Public contact

Name of contact person

1st name Kazuma
Middle name
Last name Masaki

Organization

EP Mediate Co., Ltd.

Division name

Trial Planning Section R&D Support Center Foods Department

Zip code

162-0821

Address

Kagurazaka AK Bldg., 1-8 Tsukudocho, Shinjuku-ku, Tokyo, Japan

TEL

070-4579-2569

Homepage URL


Email

masaki.kazuma026@eps.co.jp


Sponsor or person

Institute

EP Mediate Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Egao Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Medical Station Clinic Research Ethics Committee

Address

3-12-8, Takaban, Meguroku, Tokyo, Japan

Tel

03-6452-2712

Email

nakagawa.akiko297@eps.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

2022 Year 10 Month 01 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

11

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

2022 Year 07 Month 28 Day

Date of IRB

2022 Year 07 Month 28 Day

Anticipated trial start date

2022 Year 07 Month 29 Day

Last follow-up date

2022 Year 09 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

2022 Year 07 Month 29 Day

Last modified on

2023 Year 01 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000055280


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name