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Tegrenol combined with Aspirin in the Prevention of Early Neurological Deterioration of HR-NICE: A Randomized, Parallel Controlled Clinical Study

Tegrenol combined with Aspirin in the Prevention of Early Neurological Deterioration of HR-NICE: A Randomized, Parallel Controlled Clinical Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068509
Enrollment
Unknown
Registered
2023-02-21
Start date
2023-02-07
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Stroke

Interventions

TA group:Tegrelol combined with aspirin
LA group:Clopidogrel combined with aspirin

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. 40 <= age <= 70; 2. Patients with acute ischemic cerebrovascular disease within 24 hours of onset; 3. NIHSSS <= 5 in patients with cerebral infarction or ABCD2=4 in patients with TIA; 4. For patients with the first onset or previous cerebral infarction patients without sequelae such as limb paralysis, the NIHSS score will not be affected; the previous mRS score is =1 point; 5 Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Hemorrhagic stroke or mixed stroke; 2. Brain arteriovenous malformation or intracranial tumor; 3. Cardiogenic cerebrovascular disease (including but not limited to arrhythmia, atrial fibrillation, heart valve disease); 4. Patients with uncontrollable severe hypertension, severe infection or abnormal liver function, renal insufficiency, blood system diseases with bleeding tendency, etc.; 5. History of previous cerebral hemorrhage; 6. Retinal hemorrhage or visceral hemorrhage within 30 days; 7. Patients who took ticagrelor 3 months before the onset; 8. Patients with disturbance of consciousness; 9. Patients who are allergic to any component of aspirin, clopidogrel or ticagrelor; 10. Pregnant or lactating women; 11. Those who are considered by the researchers to be inappropriate to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
Incidence of early neurological deterioration;

Secondary

MeasureTime frame
NIHSS score improvement (30 days, 90 days);30 days, 90 days mRS score;Occurrence of hemorrhagic events;Blood biochemical indicators;

Countries

China

Contacts

Public ContactXiaofei Ji

The First Affiliated Hospital of Dalian Medical University

jixiaofei1979@163.com+86 180 9887 6273

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 8, 2026