Argatroban Combined With Antiplatelet Versus Antiplatelet for Acute Ischemic Stroke

Sponsor
General Hospital of Shenyang Military Region (Other)
Overall Status
Completed
CT.gov ID
NCT03552354
Collaborator
(none)
120
1
1
14.5
8.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Argatroban plus dual antiplatelet
Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
120 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Argatroban Combined With Antiplatelet Versus Antiplatelet for Acute Mild or Moderate Ischemic Stroke With Large-artery Atherosclerosis: a Prospective, Single Center Study
Actual Study Start Date :
Oct 25, 2017
Actual Primary Completion Date :
Oct 8, 2018
Actual Study Completion Date :
Jan 8, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Argatroban combined with antiplatelet

Drug: 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

Outcome Measures

Primary Outcome Measures

  1. Proportion of 1 or more increase in NIHSS [7 days]

    early neurological deterioration is defined as 1 or more increase in NIHSS

Other Outcome Measures

  1. Proportion of mRS 0-1 [90±7 days]

    the excellent outcome is defined as modifed Rankin Score (mRS) 0-1 at 90 day

  2. Proportion of mRS 0-2 [90±7 days]

    the good outcome is defined as modifed Rankin Score (mRS) 0-2 at 90 day

  3. proportion of intracranial haemorrhages [90±7 days]

    intracranial hemorrhage was defined as acute extravasation of blood into the brain parenchyma or subarachnoid space with associated neurologic symptoms

  4. proportion of organs hemorrhage [90±7 days]

    including gastrointestinal bleeding and mucocutaneous hemorrhage

  5. death [90±7 days]

    death due to any cause

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 General Hospital of Shenyang Military Region Shenyang Liaoning China 10016

Sponsors and Collaborators

  • General Hospital of Shenyang Military Region

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hui-Sheng Chen, Director of the Department, General Hospital of Shenyang Military Region
ClinicalTrials.gov Identifier:
NCT03552354
Other Study ID Numbers:
  • k(2017)38
First Posted:
Jun 11, 2018
Last Update Posted:
Jul 22, 2020
Last Verified:
Jul 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 22, 2020