UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045211
Receipt number R000051257
Scientific Title Effect of health instructions and the test food containing Salacia extract
Date of disclosure of the study information 2021/08/23
Last modified on 2022/08/22 13:48:44

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Basic information

Public title

Effect of health instructions and the test food containing Salacia extract

Acronym

Effect of health instructions and the test food containing Salacia extract

Scientific Title

Effect of health instructions and the test food containing Salacia extract

Scientific Title:Acronym

Effect of health instructions and the test food containing Salacia extract

Region

Japan


Condition

Condition

Subjects of Specific Health Guidance

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effect of health instructions and the test food containing Salacia extract

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

HbA1c, Fasting blood glucose level, Blood insulin level, HOMA-R

Key secondary outcomes

Mini Nutritional Assessment, Body weight, BMI, Abdominal circumference, N-terminal telopeptide, Osteocalcin


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food Behavior,custom

Interventions/Control_1

Health instructions for 6 months

Interventions/Control_2

Health instructions and intake of the test food containing Salacia extract for 6 months

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


Not applicable

Gender

Male and Female

Key inclusion criteria

1)Subjects of Specific Health Guidance
2)Subjects whose fasting blood glucose levels are not less than 100 mg/dL or HbA1c are not less than 5.6%
3)Subjects who have understood the purpose and contents of the study and agree to participate by signing the written informed consent

Key exclusion criteria

None

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Kazuhiro
Middle name
Last name Nishimura

Organization

Komazawa Women's University

Division name

Faculty of Human Health, Department of Health and Nutrition Sciences

Zip code

206-8511

Address

238 Sakahama, Inagi-shi, Tokyo

TEL

042-350-7111

Email

k-nishimura@komajo.ac.jp


Public contact

Name of contact person

1st name Haruka
Middle name
Last name Hamasaki

Organization

KOBAYASHI Pharmaceutical Co., Ltd.

Division name

Research & Development Dept., Healthcare Division

Zip code

567-0057

Address

1-30-3, Toyokawa, Ibaraki-city, Osaka

TEL

072-640-0131

Homepage URL


Email

h.hamasaki@kobayashi.co.jp


Sponsor or person

Institute

Komazawa Women's University

Institute

Department

Personal name



Funding Source

Organization

KOBAYASHI Pharmaceutical 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

Ryokufuso Hospital

Address

3-31-1, Hagiyama-cho, Hihashimurayama-city, Tokyo

Tel

042-392-1101

Email

keiko-5@kg7.so-net.ne.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

2021 Year 08 Month 23 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

Terminated

Date of protocol fixation

2021 Year 07 Month 26 Day

Date of IRB

2021 Year 08 Month 16 Day

Anticipated trial start date

2021 Year 08 Month 23 Day

Last follow-up date

2022 Year 03 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

2021 Year 08 Month 20 Day

Last modified on

2022 Year 08 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051257


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name