Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 2:20 PM
Ignite Modification Date: 2025-12-24 @ 2:20 PM
NCT ID: NCT04491695
Eligibility Criteria: Inclusion Criteria: 1. Acute ischemic stroke with 24 hours of symptom onset. 2. NIHSS≥4 and ≤20 points, and the paralyzed limbs is able to actively move the muscle (standardized motor examination rating scale of 2 or much higher). 3. Age 18-80 years old. 4. Informed consent obtained from patient or acceptable patient's surrogate. Exclusion Criteria: 1. Treated with intravenous or endovascular thrombectomy for the indexed acute ischemic stroke. 2. Acute ischemic stroke caused by determined or suspected cardioembolism. 3. Acute ischemic stroke caused by other determined caused, including moyamoya disease, artery dissection, arteritis, and etc. 4. Pre-stroke mRS ≥2 or the paralyzed limbs are dyskinesia before stroke. 5. Known hematochezia, gastrointestinal bleeding and any other bleeding. 6. Allergy to tirofiban or its solvents. 7. Patients suffered from severe diseases, including malignant tumor, liver cirrhosis, kidney failure, congestive heart failure, and etc. 8. Gastrointestinal or genitourinary tract bleeding within 1 years. 9. Determined coagulation disorders, platelet dysfunction, or platelet count \<100\*109/L. 10. Major surgical operation or severe trauma within 1 month. 11. Hemorrhagic retinopathy. 12. Chronic hemodialysis. 13. Uncontrolled hypertension with systolic blood pressure \>180 mmHg or diastolic blood pressure \>110 mmHg. 14. Acute pericarditis. 15. Other conditions that determined by the investigators.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 80 Years
Study: NCT04491695
Study Brief:
Protocol Section: NCT04491695