UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000013138
Receipt number R000015306
Scientific Title A Clinical Study for arteriosclerosis improvement by percutaneously absorbed lipokine
Date of disclosure of the study information 2014/02/12
Last modified on 2014/02/12 11:05:56

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

A Clinical Study for arteriosclerosis improvement by percutaneously absorbed lipokine

Acronym

A Clinical Study for arteriosclerosis improvement by percutaneously absorbed lipokine

Scientific Title

A Clinical Study for arteriosclerosis improvement by percutaneously absorbed lipokine

Scientific Title:Acronym

A Clinical Study for arteriosclerosis improvement by percutaneously absorbed lipokine

Region

Japan


Condition

Condition

metabolic syndrome

Classification by specialty

Medicine in general

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

This study examines the percutaneous absorption abilities and pharmacokinetics of macadamia nut oil with healthy volunteers.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Safety

Key secondary outcomes

Changes in blood fatty acid content
Flow Mediated Dilation(FMD)
Serum adiponectin concentration


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

20-minute massage with 10 ml of macadamia nut oil

Interventions/Control_2


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

80 years-old >

Gender

Male and Female

Key inclusion criteria

1) Patient who have metabolic syndrome or BMI 25<, obesity
2) Patients who are obtained with the prior written consent.

Key exclusion criteria

1) Patient who have a history of allergic disease.
2) Patient who had an allergic reaction in the patch test.
3) Patient who has the possibility of pregnancy, pregnancy.
4) People who have cognitive disorder (delirium, dementia and so on), schizophrenia or bipolar disorder.
5) Patients judged to be inappropriate for this study from the doctor in charge.

Target sample size

8


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Toshinori Ito

Organization

Osaka University Graduate School of Medicine

Division name

Department of Complementary and Alternative Medicine

Zip code


Address

2-2 Yamadaoka, Suita, Osaka, Japan

TEL

06-6879-3498

Email

juki@cam.med.osaka-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Miki Sakaue

Organization

Osaka University Graduate School of Medicine

Division name

Department of Complementary and Alternative Medicine

Zip code


Address

2-2 Yamadaoka, Suita, Osaka, Japan

TEL

06-6879-3498

Homepage URL


Email

mikity@cam.med.osaka-u.ac.jp


Sponsor or person

Institute

Osaka University Graduate School of Medicine
Department of Complementary and Alternative Medicine

Institute

Department

Personal name



Funding Source

Organization

Osaka University Graduate School of Medicine
Department of Complementary and Alternative Medicine

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


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

大阪大学医学部附属病院(大阪府)


Other administrative information

Date of disclosure of the study information

2014 Year 02 Month 12 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

2011 Year 11 Month 10 Day

Date of IRB


Anticipated trial start date

2011 Year 11 Month 10 Day

Last follow-up date

2013 Year 11 Month 09 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 02 Month 12 Day

Last modified on

2014 Year 02 Month 12 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015306


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name