UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000002307
Receipt number R000001078
Scientific Title Effects of granulocyte colony stimulating factor on endothelial dysfunction after implanting drug-eluting stents.
Date of disclosure of the study information 2009/08/10
Last modified on 2013/02/13 19:54:45

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Basic information

Public title

Effects of granulocyte colony stimulating factor on endothelial dysfunction after implanting drug-eluting stents.

Acronym

Effects of GCSF after implanting DES.

Scientific Title

Effects of granulocyte colony stimulating factor on endothelial dysfunction after implanting drug-eluting stents.

Scientific Title:Acronym

Effects of GCSF after implanting DES.

Region

Japan


Condition

Condition

ischemic heart disease

Classification by specialty

Cardiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy of granulocyte colony stimulating factor on accelarating reendotheliazation after implanting drug-eluting coronary stents.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Difference in recovery of endothelium dependent relaxation between GCSF group and non-GCSF group

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

YES

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

GCSF

Interventions/Control_2

Saline

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

All adult patients undergoing percutaneous coronary intervention which sirolimus-eluting stent is implanted

Key exclusion criteria

Acute myocardial infarction, revascularization of in stent restenosis,
any other contraindication of DES use

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yo Iwata

Organization

Chiba University Graduate School of Medicine

Division name

Department of Cardiovasvular Science and Medicine

Zip code


Address

1-8-1 Inohana, Chuo-ku, Chiba, Chiba, Japan

TEL

043-226-2340

Email



Public contact

Name of contact person

1st name
Middle name
Last name Yoshio Kobayashi

Organization

Chiba University Graduate School of Medicine

Division name

1-8-1 Inohana, Chuo-ku, Chiba, Chiba, Japan

Zip code


Address


TEL

043-226-2340

Homepage URL


Email



Sponsor or person

Institute

Chiba University Graduate School of Medicine Department of Cardiovascular Science and Medicine

Institute

Department

Personal name



Funding Source

Organization

Kyowa Hakko Kirin, Ltd

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

千葉大学病院 (千葉県)


Other administrative information

Date of disclosure of the study information

2009 Year 08 Month 10 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

2007 Year 10 Month 06 Day

Date of IRB


Anticipated trial start date

2008 Year 04 Month 01 Day

Last follow-up date

2011 Year 02 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2009 Year 08 Month 07 Day

Last modified on

2013 Year 02 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001078


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name