UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040665
Receipt number R000046418
Scientific Title Exploratory study on the salt discharging effect of intake Mekabu or Mozuku.
Date of disclosure of the study information 2020/06/05
Last modified on 2021/02/10 13:05:40

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Basic information

Public title

Exploratory study on the salt discharging effect of intake Mekabu or Mozuku.

Acronym

Exploratory study on the salt discharging effect of intake Mekabu or Mozuku.

Scientific Title

Exploratory study on the salt discharging effect of intake Mekabu or Mozuku.

Scientific Title:Acronym

Exploratory study on the salt discharging effect of intake Mekabu or Mozuku.

Region

Japan


Condition

Condition

Healthy Adults

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluate the salt discharging effect on Japanese (20 to 64 years old) by intake Mekabu or Mozuku for a week.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Salt intake ( urinary sodium, urinary creatinine, body weight, body height, age) at the beginning of the study or after the intake for a week.

Key secondary outcomes

Questionnaire at the beginning of the study or after the intake for a week.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Intake 35g (once a day) of Mekabu daily for a week.
Participants take test food before one of three meals.

Interventions/Control_2

Intake 40g (once a day) of Mozuku daily for a week.
Participants take test food before one of three meals.

Interventions/Control_3

none

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.Persons who received a sufficient explanation of the purpose and contents of the exam, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate with a written document.
2.Japanese who are 20 years old or more and under 65 years old.
3.Persons who highly tend to take salt at pre-questionnaire.

Key exclusion criteria

1.Persons who have chronic illness, receiving medication, have a serious disease history.
2.Persons who are allergic to the test food.
3.Persons who usually take a large amount of test food.
4.Persons who usually take medicine, specified health food, healthy food.
5.Persons who have participated in other tests within the first month before the start of the test, or those who intend to participate in another exam after consenting to this exam.
6.Persons who were judged as inappropriate for subjects by the principal investigator.
7.Persons who are pregnant, planning or hoping to be pregnant during the study period, breastfeeding.

Target sample size

90


Research contact person

Name of lead principal investigator

1st name Hirohito
Middle name
Last name Ishikawa

Organization

Healthcare Systems Co., Ltd.

Division name

Research and Development Department

Zip code

105-0004

Address

Nisshin Tatemono Shinbashi Bld. 7F, 4-6-15 Shinbashi, Minato-ku, Tokyo, JAPAN

TEL

03-5562-8825

Email

ishikawa@hc-sys.jp


Public contact

Name of contact person

1st name Yukari
Middle name
Last name Kobayashi

Organization

Healthcare Systems Co., Ltd.

Division name

Sales Planning Department

Zip code

105-0004

Address

Nisshin Tatemono Shinbashi Bld. 7F, 4-6-15 Shinbashi, Minato-ku, Tokyo, JAPAN

TEL

070-1450-5470

Homepage URL


Email

kobayashi@hc-sys.jp


Sponsor or person

Institute

Healthcare Systems Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

KANERYO Sea Vegetable Corporation

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

The Ethics Committee of Healthcare Systems Co., Ltd.

Address

Nisshin Tatemono Shinbashi Bld. 7F, 4-6-15 Shinbashi, Minato-ku, Tokyo, JAPAN

Tel

03-6809-2722

Email

soumu@hc-sys.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 06 Month 05 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

90

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 05 Day

Date of IRB

2020 Year 06 Month 05 Day

Anticipated trial start date

2020 Year 06 Month 25 Day

Last follow-up date

2020 Year 12 Month 31 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 06 Month 05 Day

Last modified on

2021 Year 02 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046418


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name