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Argatroban Combined With Antiplatelet Versus Antiplatelet for Acute Ischemic Stroke

G

General Hospital of Northern Theater Command of Chinese People's Liberation Army

Status and phase

Completed
Phase 4

Conditions

Stroke, Ischemic

Treatments

Drug: Argatroban plus dual antiplatelet

Study type

Interventional

Funder types

Other

Identifiers

NCT03552354
k(2017)38

Details and patient eligibility

About

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.

Enrollment

120 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

120 participants in 1 patient group

Argatroban combined with antiplatelet
Experimental group
Treatment:
Drug: Argatroban plus dual antiplatelet

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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