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The relationship between Aspirin resistance and glycoprotein IIIa polymorphism in recurrent atherosclerosis ischemic stroke

The relationship between Aspirin resistance and glycoprotein IIIa polymorphism in recurrent atherosclerosis ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-17010810
Enrollment
Unknown
Registered
2017-03-07
Start date
2017-04-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atherosclerosis ischemic stroke

Interventions

non-aspirin resistance:oral aspirin or change other antiplatelet strategy
aspirin resistance:oral aspirin or change other antiplatelet strategy
CC and CT group:oral aspirin or change other antiplatelet strategy
control group (TT group):oral aspirin or change other antiplatelet strategy

Sponsors

Lanzhou General Hospital of Lanzhou Military Area Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. aged 45 years old and more; 2. Patients who had been diagnosed atherosclerosis ischemic stroke must have had a recurrent stroke which defines transient ischemia attach(TIA), ischemic stroke or silence stroke. Magnetic resonance/computerized tomography can find the new ischemic Lesions; 3. Have taken aspirin for more than 24 hours; 4. All subjects must be volunteers and willing to sign the written informed consent.

Exclusion criteria

Exclusion criteria: 1. Acute cerebral ischemic events is deriving from non- atherosclerosis ischemic stroke(Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria (II, IV, V)); 2. Subjects with the symptoms of neurological impairment without evidence of acute infarction on baseline CT or MRI of the head; 3. Exclude below diseases such as intracerebral hemorrhage, vascular malformation, tumor, abscess and so on; 4. Subjects with documented history of any gastrointestinal disorders or other organs bleeding or major surgery within the previous 3 months; 5. Subjects with any coagulation, bleeding or blood disorders; 6. Subjects, who have received heparin therapy, oral anticoagulation therapy or other antiplatelet drugs before randomization; 7. Subjects who have had treatment with thrombolysis around the time of randomization; 8. Subjects who have had endovascular stent in cervical or intracranial artery and oral dual antiplatelet drugs before randomization; 9. Subjects who are contraindicated in aspirin as well as any of their components.

Design outcomes

Primary

MeasureTime frame
glycoprotein IIIa polymorphism;Platelet aggregation rate;recurrent ischemic stroke;intracerebral hemorrhage;mortality rate;

Secondary

MeasureTime frame
NIHSS;brain CT or MRI;

Countries

China

Contacts

Public ContactRong Yin

Department of Neurology, Lanzhou General Hospital of Lanzhou Military Area Command

yin_rong_@163.com+86 13919930466

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026