UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020272
Receipt number R000023403
Scientific Title Bioequivalence study of the consumption of plant-derived processed product with anti-obesity in healthy adults
Date of disclosure of the study information 2016/01/20
Last modified on 2019/08/26 14:52:51

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Basic information

Public title

Bioequivalence study of the consumption of plant-derived processed product with anti-obesity in healthy adults

Acronym

Bioequivalence study of plant-derived processed product in healthy adults.

Scientific Title

Bioequivalence study of the consumption of plant-derived processed product with anti-obesity in healthy adults

Scientific Title:Acronym

Bioequivalence study of plant-derived processed product in healthy adults.

Region

Japan


Condition

Condition

Healthy subjects

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the bioequivalence of original product A-001and generic product A-002

Basic objectives2

Bio-equivalence

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

AUC0-8hr and Cmax of postprandial triglyceride

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Product code A-002(1day, 1time, 10g), washout(over 6days), product code A-001(1day, 1time, 10g)

Interventions/Control_2

Product code A-001(1day, 1time, 10g), washout(over 6days), product code A-002(1day, 1time, 10g)

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

35 years-old <=

Age-upper limit

65 years-old >

Gender

Male and Female

Key inclusion criteria

1)BMI>=23.0and<30.0 kg/m2
2)Age>=35 and<65 years old
3)Person who provides inforrned
consent by a document

Key exclusion criteria

1) individual with liver, kidney and heart disease, or disorder of respiration, endocrine, metabolism, nervous system, consciousness, or diabetes, or other diseases, 2) individual given surgery within 2 months before the trial, 3) medicine user for hyperglycaemia, lipidemia, or hypertension, 4) individual intakes supplements or the food for specific use of health authorized the government, 5) individual experienced unpleasant feeling during blood drawing, 6) individual donated 200 mL or more blood within 1 month before the trial, 7) heavy smoker (cigarettes>=21/day), 8) shiftworker, 9) individual plans bussiness trip for 10 consecutive days or more, 10) individual had allergy against any constituents in the test diet, 11) individual can not conform to record of daily diet for 6 days (3 days x 2 times), 12) individual cannot allow operator to consult his/her data of the past health check, 13) individual have already participated other clinical trial and will participate, 14) pregnant women or breast-feeding women, 15) individual who was judged ineligibles by clinician in this trial

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Shinichiro
Middle name
Last name Saito

Organization

Kao Corporation

Division name

Health Care Food Research Labs.

Zip code

131-6501

Address

2-1-3 Bunka Sumida-ku Tokyo

TEL

03-5630-7456

Email

shoji.kentaro@kao.co.jp


Public contact

Name of contact person

1st name Shinpei
Middle name
Last name Tomita

Organization

New Drug Research Center, Inc.

Division name

Clinical Research Dept.

Zip code

061-1405

Address

452-1 Toiso, Eniwa-shi, Hokkaido

TEL

0123-34-0412

Homepage URL


Email

s-tomita@ndrcenter.co.jp


Sponsor or person

Institute

New Drug Research Center, Inc.

Institute

Department

Personal name



Funding Source

Organization

Kao 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 Review Board of Miyawaki Orthopedic Hospital

Address

3-1-6 Ariake-cho, Eniwa city, Hokkaido

Tel

0123-33-4026

Email

d-kameda@mediffom.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

福原医院


Other administrative information

Date of disclosure of the study information

2016 Year 01 Month 20 Day


Related information

URL releasing protocol

Unpublished due to the protocol including the intellectual property rights

Publication of results

Published


Result

URL related to results and publications

works in progress

Number of participants that the trial has enrolled

17

Results

he result suggested that there was bioequivalence between test food and control food.

Results date posted

2019 Year 08 Month 26 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

Healthy subjects

Participant flow

20 participants completed and 17 subjects were incorporated into the analyses

Adverse events

No adverse effect related to the test diets reported

Outcome measures

AUC0-8hr and Cmax of postprandial triglyceride

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Main results already published

Date of protocol fixation

2015 Year 12 Month 15 Day

Date of IRB

2015 Year 12 Month 15 Day

Anticipated trial start date

2016 Year 01 Month 24 Day

Last follow-up date

2016 Year 04 Month 14 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 12 Month 18 Day

Last modified on

2019 Year 08 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023403


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name