UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000059192
Receipt number R000067624
Scientific Title A study to examine the effects of intake of a capsule containing multi-ingredient(FD-2553) on fat metabolism
Date of disclosure of the study information 2025/11/30
Last modified on 2025/09/24 11:36:02

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Basic information

Public title

A study to examine the effects of intake of a capsule containing multi-ingredient(FD-2553) on fat metabolism

Acronym

A study to examine the effects of intake of a capsule containing multi-ingredient(FD-2553) on fat metabolism

Scientific Title

A study to examine the effects of intake of a capsule containing multi-ingredient(FD-2553) on fat metabolism

Scientific Title:Acronym

A study to examine the effects of intake of a capsule containing multi-ingredient(FD-2553) on fat metabolism

Region

Japan


Condition

Condition

Healthy volunteers

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effects of intake of the test food on fat metabolism

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Fat metabolism equivalent to physical activity intensity

Key secondary outcomes

Respiratory quotient


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Single intake of the test food -> washout period (1 week) -> Single intake of the placebo

Interventions/Control_2

Single intake of the placebo -> washout period (1 week) -> Single intake of the test food

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

20 years-old <=

Age-upper limit

45 years-old >=

Gender

Male

Key inclusion criteria

1)Male whose age of 20 to 45
2)Person whose BMI of 18.5 kg/m2 or more and less than 25.0 kg/m2
3)Person with no regular exercise habit of twice a week or more
4)Person receiving sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntarily participate in the study and being able to personally sign a written informed consent
5)Person who can have examinations at the specified date

Key exclusion criteria

1)Person receiving a medical treatment for serious cardio-vascular, hepatic, renal, respiratory, endocrine or metabolic disorders or having a medical history of these disorders
2)Person having a medical history of chest pain or syncope
3)Person having low back pain, arthralgia, lumber hernia, disease of lower limbs or palpitations
4)Person who may have allergic symptoms to the test food or standardized diet
5)Person having moderate or more allergic rhinitis
6)Person who regularly take medicines and quasi-drugs that affect energy metabolism
7)Person who regularly take Foods with Function Claims indicating functions that affect energy metabolism
8)Person who have a smoking habit (including heated tobacco and electronic cigarettes)
9)Person who consume excessive alcohol (equivalent to an average of 40 g or more of pure alcohol per day)
10)Person who restrict carbohydrates intake
11)Person working night shift or day-night shift
12)Person who have donated more than 200 ml of blood within 1 month, or more than 400 ml within 3 months prior to the start of the present study
13)Person who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study
14)Person deemed unsuitable by the investigator

Target sample size

24


Research contact person

Name of lead principal investigator

1st name Takashi
Middle name
Last name Tagawa

Organization

Maruzen Pharmaceuticals Co., Ltd

Division name

Research & Development Division

Zip code

729-3102

Address

1089-8, Shinichi-cho Sagata, Fukuyama, Hiroshima

TEL

0847-52-6262

Email

t-tagawa@maruzenpcy.co.jp


Public contact

Name of contact person

1st name Tomohiro
Middle name
Last name Sugino

Organization

Soiken Inc.

Division name

R&D Division

Zip code

560-0082

Address

Senri Life Science Center 13F, 1-4-2, Shinsenri-higashimachi, Toyonaka, Osaka

TEL

06-6871-8888

Homepage URL


Email

sugino@soiken.com


Sponsor or person

Institute

Maruzen Pharmaceuticals Co., Ltd

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

IRB of Fukuda Clinic

Address

Shin-Osaka brick building 2F, 1-6- 1 Miyahara, Yodogawa, Osaka, Osaka

Tel

06-6398-0203

Email

fukudaclinicIRB@gmail.com


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

2025 Year 11 Month 30 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

2025 Year 08 Month 16 Day

Date of IRB

2025 Year 08 Month 16 Day

Anticipated trial start date

2025 Year 12 Month 04 Day

Last follow-up date

2025 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

2025 Year 09 Month 25 Day

Last modified on

2025 Year 09 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067624