UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000021840
Receipt number R000025183
Scientific Title Adhibition for Clopidogrel loading dose in acute ischemic stroke
Date of disclosure of the study information 2016/04/12
Last modified on 2018/10/10 15:13:19

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Basic information

Public title

Adhibition for Clopidogrel loading dose in acute ischemic stroke

Acronym

CLD in stroke

Scientific Title

Adhibition for Clopidogrel loading dose in acute ischemic stroke

Scientific Title:Acronym

CLD in stroke

Region

Japan


Condition

Condition

Acute ischemic stroke

Classification by specialty

Neurology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Test the efficacy and safety of oral clopidogrel 300 mg administration

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Hemorrhagic complication and recurrent stroke of the start of the onset of ischemic stroke within three weeks.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Clopidogrel 300 mg

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

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Acute ischemic stroke patients within three days

Key exclusion criteria

pancytopenia
severe liver dysfunction and/or renal dysfunction
hemorrhagic transformation in brain CT or MRI
active hemorrhagic lesion

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kazuo Kitagaza

Organization

Tokyo Women's Medical University

Division name

Department of Neurology

Zip code


Address

Kawada-cho 8-1, Shinjuku-ku, Tokyo, Japan.

TEL

03-3353-8111

Email

kkitagawa@nij.twmu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Sono Toi

Organization

Tokyo Women's Medical University

Division name

Department of Neurology

Zip code


Address

Kawada-cho 8-1, Shinjuku-ku, Tokyo, Japan.

TEL

+81-3-3353-8111

Homepage URL


Email

stoi@nij.twmu.ac.jp


Sponsor or person

Institute

Department of Neurology, Tokyo Women's Medical University

Institute

Department

Personal name



Funding Source

Organization

Department of Neurology, Tokyo Women's Medical University

Organization

Division

Category of Funding Organization

Other

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

東京女子医科大学 神経内科


Other administrative information

Date of disclosure of the study information

2016 Year 04 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

Enrolling by invitation

Date of protocol fixation

2016 Year 03 Month 18 Day

Date of IRB


Anticipated trial start date

2016 Year 04 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



Management information

Registered date

2016 Year 04 Month 08 Day

Last modified on

2018 Year 10 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025183


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name