UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000003426
Receipt number R000004145
Scientific Title Genomic and functional evaluation of perivascular adipose tissue.
Date of disclosure of the study information 2010/04/05
Last modified on 2014/03/27 16:01:26

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Basic information

Public title

Genomic and functional evaluation of perivascular adipose tissue.

Acronym

Genomic and functional evaluation of perivascular adipose tissue.

Scientific Title

Genomic and functional evaluation of perivascular adipose tissue.

Scientific Title:Acronym

Genomic and functional evaluation of perivascular adipose tissue.

Region

Japan


Condition

Condition

Atherosclerosis

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

YES


Objectives

Narrative objectives1

To clarify the influence of perivascular adipose tissue to the formation of atherosclerosis of patients with cardiovascular disease.

Basic objectives2

Others

Basic objectives -Others

To identify the vasodilatative molecule from perivascular adipose tissue

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Adipocytokines from perivascular adipose tissue.

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who undergo cardiovascular surgery in Tokushima University Hospital, Tokushima Prefectural Central Hospital, Ehime Prefectural Central Hospital, Sakakibara Memorial Hospital.

Key exclusion criteria

Patients from whom written informed consent was not obtained.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Masataka Sata

Organization

University of Tokushima Graduate School, Institute of Health Bioscience.

Division name

Department of cardiovascular medicine

Zip code


Address

3-18-15 Kuramoto-cho, Tokushima-city, Tokushima 770-8503, Japan

TEL

088-633-7851

Email

masataka.sata@tokushima-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Michio Shimabukuro

Organization

University of Tokushima Graduate School, Institute of Health Bioscience.

Division name

Department of cardiovascular medicine

Zip code


Address

3-18-15 Kuramoto-cho, Tokushima-city, Tokushima 770-8503, Japan

TEL

088-633-7851

Homepage URL


Email

mshimabukuro-ur@umin.ac.jp


Sponsor or person

Institute

Department of Cardiovascular Medicine, University of Tokushima Graduate School, Institute of Health Bioscience

Institute

Department

Personal name



Funding Source

Organization

Knowledge Cluster and New Research Area

Organization

Division

Category of Funding 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

徳島大学医学部・歯学部附属病院


Other administrative information

Date of disclosure of the study information

2010 Year 04 Month 05 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

Open public recruiting

Date of protocol fixation

2008 Year 09 Month 22 Day

Date of IRB


Anticipated trial start date

2008 Year 09 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Pare samples are obtained from epicardial and subcutaneous adipose tissue during elective cardiac surgery. Inflammatory
cell infiltration is investigated by immunohistochemical staining. Expression of adipocytokines was evaluated by real-time
quantitative reverse transcription-polymerase chain reaction.


Management information

Registered date

2010 Year 04 Month 01 Day

Last modified on

2014 Year 03 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000004145


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name