UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000051505
Receipt number R000058713
Scientific Title Effects of the intake of foods containing ginger on the swelling
Date of disclosure of the study information 2023/07/10
Last modified on 2025/01/06 08:23:34

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Basic information

Public title

Effects of the intake of foods containing ginger on the swelling

Acronym

Effects of the intake of foods containing ginger on the swelling

Scientific Title

Effects of the intake of foods containing ginger on the swelling

Scientific Title:Acronym

Effects of the intake of foods containing ginger on the swelling

Region

Japan


Condition

Condition

Healthy Japanese subjects

Classification by specialty

Plastic surgery Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To verify the effects of the intake of foods containing ginger on the intestinal swelling in healthy Japanese subjects.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Lower limb volume

Key secondary outcomes

Skin surface temperature, Blood flow


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

Treatment

Type of intervention

Food

Interventions/Control_1

Intake of ginger cupsule (single round), Washout period (more than 1 weeks), Intake of placebo cupsule (single round)

Interventions/Control_2

Intake of placebo cupsule (single round), Washout period (more than 1 weeks), Intake of ginger cupsule (single round)

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. Japanese males and females aged over 18 years old at the time of informed consent.
2. Subjects who agree to participate in this study with a written informed consent after receiving sufficient explanation relating to this study.

Key exclusion criteria

none

Target sample size

10


Research contact person

Name of lead principal investigator

1st name Motoko
Middle name
Last name Takaoka

Organization

Kobe College

Division name

School of Human Sciences

Zip code

662-8505

Address

4-1, Okadayama, Nishinomiya-city, Hyogo, Japan

TEL

0798-51-8668

Email

takaoka@mail.kobe-c.ac.jp


Public contact

Name of contact person

1st name Motoko
Middle name
Last name Takaoka

Organization

Kobe College

Division name

School of Human Sciences

Zip code

662-8505

Address

4-1, Okadayama, Nishinomiya-city, Hyogo, Japan

TEL

0798-51-8668

Homepage URL


Email

takaoka@mail.kobe-c.ac.jp


Sponsor or person

Institute

Kobe College

Institute

Department

Personal name



Funding Source

Organization

Ikeda Food Research 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

Kobe college school of human sciences research ethics committee

Address

4-1, Okadayama, Nishinomiya-city, Hyogo, Japan

Tel

0798-51-8423

Email

sumi@mail.kobe-c.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

2023 Year 07 Month 10 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

10

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

2023 Year 04 Month 11 Day

Date of IRB

2023 Year 04 Month 11 Day

Anticipated trial start date

2023 Year 05 Month 15 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2024 Year 03 Month 10 Day


Other

Other related information



Management information

Registered date

2023 Year 07 Month 03 Day

Last modified on

2025 Year 01 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000058713