Argatroban Combined With Antiplatelet Versus Antiplatelet for Acute Ischemic Stroke

NCT ID: NCT03552354

Last Updated: 2020-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-25

Study Completion Date

2019-01-08

Brief Summary

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Intravenous thrombolysis is considered as the first choice for ischemic stroke. In the recent years, endovascular therapy is demonstrated to be effective to treat ischemic with big vessel occlusion. However, only a minority of patients can get intravenous thrombolysis or endovascular therapy due to the restricted time window and strict indications. Dual antiplatelet has been demonstrated to be effective in the patients with high risk of TIA or minor ischemic stroke (NIHSS\<4). But there is still stroke progression although dual antiplatelet. The ischemic stroke patients with NIHSS \> 3 has been recommended to give aspirin in most guidelines. Of those patients, mild to moderate stroke patients (3\<NIHSS\<10) will result in the poor outcomes if the progression occurs. In addition, large artery atherosclerosis (LAA) stroke is prone to progress. So, we argue that the mild to moderate stroke with LAA should be give more intensive antiplatelet. In the present study, argatroban combined with antiplatelet therapy (3-5 days) is used to treat the proposed patients to investigate the safety and effectiveness.

Detailed Description

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Conditions

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Stroke, Ischemic

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Argatroban combined with antiplatelet

Group Type EXPERIMENTAL

Argatroban plus dual antiplatelet

Intervention Type DRUG

A continuous argatroban infusion of 1.0 ug/kg per minute for 2-5 days adjusted to a target activated partial thromboplastin time of 1.75 X baseline (about 10%). For the first day, clopidogrel with loading dose 300mg, and aspirin 100mg were given, and followed by clopidogrel 75 mg and aspirin 100mg each day

Interventions

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Argatroban plus dual antiplatelet

A continuous argatroban infusion of 1.0 ug/kg per minute for 2-5 days adjusted to a target activated partial thromboplastin time of 1.75 X baseline (about 10%). For the first day, clopidogrel with loading dose 300mg, and aspirin 100mg were given, and followed by clopidogrel 75 mg and aspirin 100mg each day

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Age 18-80 years old;
2. Clear diagnosis of ischemic stroke patients with head CT or MRI examination;
3. The time of onset is less than 72 hours;
4. NIHSS score is less than 12 points;
5. the large artery atherosclerosis etiology
6. Signed informed consent.

Exclusion Criteria

1. Hemorrhagic stroke or mixed stroke;
2. Patients with planned thrombolytic therapy;
3. Serious diseases such as severe infection or liver, kidney, hematopoietic system, endocrine system, etc.;
4. The history of stroke and had serious sequelae (mRS\> 1);
5. Allergic to aspirin/clopidogrel and argatroban;
6. ischemic stroke caused by other causes, such as small vessel lesions, cardiogenic embolism, arterial dissection, vasculitis and other cerebral infarction;
7. Previous history of cerebral hemorrhage;
8. It is expected to use other anti-platelet agents or non-steroidal anti-inflammatory agents that affect platelet function;
9. within 3 months of gastrointestinal bleeding or major surgery;
10. any unqualified patients judged by researchers.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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General Hospital of Shenyang Military Region

OTHER

Sponsor Role lead

Responsible Party

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Hui-Sheng Chen

Director of the Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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General Hospital of Shenyang Military Region

Shenyang, Liaoning, China

Site Status

Countries

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China

Other Identifiers

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k(2017)38

Identifier Type: -

Identifier Source: org_study_id

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