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:
2026-03-26 @ 3:17 PM
Ignite Modification Date:
2026-03-26 @ 3:17 PM
NCT ID:
NCT07322835
Eligibility Criteria:
Inclusion Criteria:
1. Age \>18 year
2. Pre-stroke mRS ≤1
3. Diagnosis of ischemic stroke, confirmed by imaging (CT or MRI)
4. Stroke onset or last seen well (LSW) to visit ≤ 24h
5. NIHSS ≤ 5
6. Receive standard medication or IVT (TNK or rtPA) ± EVT, or EVT alone; for IVT beyond standard time window, initiation of treatment must occur within 4.5-24h of last seen well and ASPECTs≥7 or Perfusion lesion-ischemic core mismatch (ischemic core volume \<70mL, mismatch rate \>1.2, mismatch volume \>10mL or mismatch between the presence of an abnormal signal on DWI and no visible signal change on FLAIR)
7. Patients or their eligible surrogates provided informed consent
Exclusion Criteria:
1. Pregnant or breastfeeding women
2. Patients who already received reperfusion therapy for the current stroke before arriving at the hospital
3. Participation in another interventional clinical trial that could interfere with the outcomes of this study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07322835
Study Brief:
Protocol Section:
NCT07322835