UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000005223
Receipt number R000006206
Scientific Title Effects of green tea extract high in catechins on obese subjects
Date of disclosure of the study information 2011/03/14
Last modified on 2019/07/25 06:23:40

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Basic information

Public title

Effects of green tea extract high in catechins on obese subjects

Acronym

Effects of tea catechins on obesity.

Scientific Title

Effects of green tea extract high in catechins on obese subjects

Scientific Title:Acronym

Effects of tea catechins on obesity.

Region

Japan


Condition

Condition

obesity

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The body fat reducing effect and reduction of risk for cardiovascular disease by continuous ingestion of a green tea extract high in catechins were investigated in humans with typical lifestyles.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Body weight, body mass index, body fat ratio, body fat mass, waist circumference, hip circumference, abdominal visceral fat area, and abdominal subcutaneous fat area

Key secondary outcomes

Blood pressure and serum low-density lipoprotein cholesterol.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Dose comparison

Stratification

YES

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

No need to know


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

Catechin beverage (containing 582.8mg of catechins) 1 can per day for 12 weeks.

Interventions/Control_2

Control beverage (containing 96.3mg of catechins) 1 can per day for 12 weeks.

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

25 years-old <=

Age-upper limit

55 years-old >=

Gender

Male and Female

Key inclusion criteria

Healthy Japanese women and men 25 to 55 years age with body mass index of 24 to 30 kg/m^2 and/or waist circumference of 80 to 94cm.

Key exclusion criteria

Serious liver disease
Serious renal disease

Target sample size

270


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takashi Tsuchida

Organization

Isogo Central Hospital

Division name

Center of health examination.

Zip code


Address

2-20-45, Isogo Isogo-ku Yokohama Japan

TEL

045-752-1217

Email



Public contact

Name of contact person

1st name
Middle name
Last name Kazuya Kozuma

Organization

Kao Corporation

Division name

Health Care Food Research Labs.

Zip code


Address

2-1-3, Bunka Sumida-ku Tokyo Japan

TEL

03-5630-7268

Homepage URL


Email

kouzuma.kazuya@kao.co.jp


Sponsor or person

Institute

Esucal Laboratories

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


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

磯子中央病院(神奈川県)、児玉中央病院(埼玉県)、セントラル病院(東京都)、厚生病院(東京都)、中山産婦人クリニック(埼玉県)、久野マインズタワークリニック(東京都)、亀戸駅前クリニック(東京都)


Other administrative information

Date of disclosure of the study information

2011 Year 03 Month 14 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results

RESULTS: Data were analyzed using per-protocol samples of 240 subjects (catechin group; n = 123, control group; n = 117). Decreases in body weight, body mass index, body fat ratio, body fat mass, waist circumference, hip circumference, visceral fat area, and subcutaneous fat area were found to be greater in the catechin group than in the control group. A greater decrease in systolic blood pressure (SBP) was found in the catechin group compared with the control group for subjects whose initial SBP was 130 mm Hg or higher. Low-density lipoprotein (LDL) cholesterol was also decreased to a greater extent in the catechin group. No adverse effect was found.
DISCUSSION: The continuous ingestion of a green tea extract high in catechins led to a reduction in body fat, SBP, and LDL cholesterol, suggesting that the ingestion of such an extract contributes to a decrease in obesity and cardiovascular disease risks.
Obesity. 2007;15(6):1473-1483.

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

Main results already published

Date of protocol fixation

2002 Year 04 Month 18 Day

Date of IRB

2002 Year 04 Month 18 Day

Anticipated trial start date

2002 Year 04 Month 01 Day

Last follow-up date

2002 Year 08 Month 01 Day

Date of closure to data entry

2002 Year 10 Month 01 Day

Date trial data considered complete

2002 Year 11 Month 01 Day

Date analysis concluded

2002 Year 11 Month 01 Day


Other

Other related information



Management information

Registered date

2011 Year 03 Month 09 Day

Last modified on

2019 Year 07 Month 25 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006206


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name