UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000033832
Receipt number R000038587
Scientific Title Investigation of promoting osteogenesis by intake of vitamin K2-rich Natto
Date of disclosure of the study information 2018/08/21
Last modified on 2018/08/21 11:06:23

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Basic information

Public title

Investigation of promoting osteogenesis by intake of vitamin K2-rich Natto

Acronym

Investigation of promoting osteogenesis by intake of vitamin K2-rich Natto

Scientific Title

Investigation of promoting osteogenesis by intake of vitamin K2-rich Natto

Scientific Title:Acronym

Investigation of promoting osteogenesis by intake of vitamin K2-rich Natto

Region

Japan


Condition

Condition

Healthy Adult

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Promoting osteogenesis and improving bone metabolism function when feeding Natto for 6 weeks

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Blood (osteocalcin)

Key secondary outcomes

Urine (Type I collagen cross-linked N- telopeptide),
Urine (deoxypyridinoline),
Blood (vitamin K2)


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

Treatment

Type of intervention

Food

Interventions/Control_1

Natto

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

40 years-old <=

Age-upper limit

64 years-old >=

Gender

Female

Key inclusion criteria

Postmenopausal women of ages 40 to 64 years old

Key exclusion criteria

1. Persons who has liver disease, renal disease, digestive organ disease, heart trouble, peripheral vascular disorder, a person with a history of the past that may have an influence on other final examination results or person with a history of the operation
2. Person who take warfarin
3. Persons who liver function and renal function test values show abnormalities
4. Currently, those with a disorder under treatment
5. Persons who have food or drug allergy
6. Person who suffer from anemia
7. Persons who do intense sports or are on a diet
8. Persons who can't stop using functional foods (including Food for Specified Health Uses or Foods with Function Claims) and/or Specified quasi-drugs during the current study periods
9. Persons who are taking healthfoods, quasi medical items, medicines (including OTC, prescription medicine) containing ingredients contained in the test food
10. Persons who consume excess alcohol or can not abstinence from the day before the test until the day
11. Persons who are pregnant, or persons who are planning to become pregnant or breastfeeding during the study period
12. Persons who are participating in the other study or planning to participate during the study period
13. Persons who judged inappropriate by the study responsible doctor for other reasons

Target sample size

15


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Naoki Miura

Organization

Miura Clinic, Medical Corporation Kanonkai

Division name

Internal Medicine

Zip code


Address

9F Higashitenma Bldg.,1-7-17 Higashitenma, Kita-ku, Osaka-shi, Osaka, Japan

TEL

06-6135-5200

Email

info@miura-cl.jp


Public contact

Name of contact person

1st name
Middle name
Last name Makoto Terashima

Organization

Oneness Support Co., Ltd.

Division name

Clinical trial Division

Zip code


Address

9F Higashitenma Bldg.,1-7-17 Higashitenma, Kita-ku, Osaka-shi, Osaka, Japan

TEL

06-4801-8917

Homepage URL


Email

mterashima@miura-cl.jp


Sponsor or person

Institute

Takanofoods Co., Ltd.

Institute

Department

Personal name



Funding Source

Organization

Takanofoods Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor

Miura Clinic, Medical Corporation Kanonkai
Oneness Support Co., Ltd.

Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2018 Year 08 Month 21 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

2018 Year 08 Month 18 Day

Date of IRB


Anticipated trial start date

2018 Year 08 Month 23 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 08 Month 21 Day

Last modified on

2018 Year 08 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000038587