UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029871
Receipt number R000034077
Scientific Title Clinical study of low molecular Fish collagen peptide. A randomized, placebo-controlled double-blind study using low molecular fish collagen peptide in healthy adults suffering from occasional knee pain and discomfort -Verification of influence on knee joint function by continuous ingestion of low molecular fish collagen peptide-
Date of disclosure of the study information 2017/11/08
Last modified on 2023/05/15 09:48:46

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Basic information

Public title

Clinical study of low molecular Fish collagen peptide.
A randomized, placebo-controlled double-blind study using low molecular fish collagen peptide in healthy adults suffering from occasional knee pain and discomfort
-Verification of influence on knee joint function by continuous ingestion of low molecular fish collagen peptide-

Acronym

Clinical study of low molecular Fish collagen peptide.

Scientific Title

Clinical study of low molecular Fish collagen peptide.
A randomized, placebo-controlled double-blind study using low molecular fish collagen peptide in healthy adults suffering from occasional knee pain and discomfort
-Verification of influence on knee joint function by continuous ingestion of low molecular fish collagen peptide-

Scientific Title:Acronym

Clinical study of low molecular Fish collagen peptide.

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to verify the influence of 12weeks ingestion of low molecular fish collagen peptide to the function of knee joint.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

VAS survey

Key secondary outcomes

VAS survey
The knee joint function survey
Life Style survey


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

YES

Dynamic allocation


Institution consideration

Institution is not considered as adjustment factor.

Blocking


Concealment

No need to know


Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Ingestion of low molecular weight of fish collagen peptide for 12 weeks.

Interventions/Control_2

Ingestion of placebo 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

45 years-old <=

Age-upper limit

75 years-old >

Gender

Male and Female

Key inclusion criteria

1.
The age, more than 45 years old, less than 75 years old, Healthy adult male and female.
2.
A joint of the knee is uncomfortable feeling. But Medicine treatment isn't being performed.
3.
The person who is giving written informed consent.

Key exclusion criteria

1.
The person is the knee arthritis and has a medical treatment by a doctor.
The person diagnosed with osteoarthritis of the knee.
2.
The person infected with cerebrovascular disease, a heart disease, a liver disease, a kidney disease and a digestive organ disease
The person who judged that a trouble had the above medical history in clinical test participation
3.
The person is allergy to medication and/or food.
The person diagnosed with atopic dermatitis.
4.
The person who had abnormality in the blood pressure and the laboratory test etc. in a screening.
5.
The person who is taking healthy food and a supplement (hyaluronic acid, glucosamine etc.), and can't stop intake of these in the test duration.
6.
The person who is started new medical treatment within 1week before intake the test food.
The person who is plan to undergo medical treatment on knees during the study.
7.
The person who judged that a test responsibility PI was disqualified.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Director, Mikio Chibana,M.D.

Organization

OROKU HEART CLINIC

Division name

N.A.

Zip code


Address

1-12-2,Akamine,Nha-shi,Okinawa,901-0154,Japan

TEL

098-852-8080

Email

ren-ccrc@umin.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Director, Mikio Chibana,M.D.

Organization

OROKU HEART CLINIC

Division name

N.A.

Zip code


Address

1-12-2,Akamine,Nha-shi,Okinawa,901-0154,Japan

TEL

098-852-8080

Homepage URL


Email

ren-ccrc@umin.ac.jp


Sponsor or person

Institute

OROKU HEART CLINIC

Institute

Department

Personal name



Funding Source

Organization

Medicos International,Inc.

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



Other administrative information

Date of disclosure of the study information

2017 Year 11 Month 08 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

Completed

Date of protocol fixation

2017 Year 11 Month 01 Day

Date of IRB

2017 Year 10 Month 30 Day

Anticipated trial start date

2017 Year 11 Month 08 Day

Last follow-up date

2018 Year 02 Month 18 Day

Date of closure to data entry

2018 Year 03 Month 03 Day

Date trial data considered complete

2018 Year 03 Month 11 Day

Date analysis concluded

2018 Year 05 Month 28 Day


Other

Other related information



Management information

Registered date

2017 Year 11 Month 08 Day

Last modified on

2023 Year 05 Month 15 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034077


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name