Phase
Condition
Cardiac Ischemia
Stroke
Thrombosis
Treatment
Tenecteplase
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age ≥18 years;
Medium vessel occlusion (MeVO), referring to M2-3 of MCA; A1-3 of ACA; P1-3 of PCA;PICA, AICA or SCA (including primary, distal embolism in the same region afterthrombectomy or concurrent embolism in other regions).
Primary MeVO as detected by the first DSA examination or secondary MeVO aftermechanical thrombectomy for large vessel occlusion;
MeVO causes neurological deficits in motor strength, language, vision etc;
Endovascular mechanical thrombectomy cannot be performed as assessed by theinvestigator;
Absence of parenchymal hematoma on CT images performed in the angio suite.
Within 24 hours from symptom onset;
Signed informed consent by patient or patient's legally authorized representative.
Exclusion
Exclusion Criteria:
Patients with completed infarction in the territory of the MeVO on non-contrast CT;
Patients with intracranial hemorrhage;
Coagulation disorders, tendency for systemic hemorrhagic, thrombocytopenia (<100,000/mm3);
Severe hepatic or renal dysfunction, increase in ALT or AST (more than 2 times ofupper limit of normal value), increase in serum creatinine (more than 1.5 times ofupper limit of normal value) or requiring dialysis;
After mechanical thrombectomy, severe and sustained (> 5 minutes) uncontrolledhypertension (systolic blood pressure over 180mmHg or diastolic blood pressure over 105 mmHg);
Patients with contraindication or allergy to any ingredient of study medication;
Pregnancy, plan to get pregnant or active lactation;
The estimated life expectancy is less than 6 months due to other serious diseases;
Other conditions unsuitable for this clinical study as assessed by researcher.
Study Design
Connect with a study center
General Hospital of Northern Theater Command
ShenYang, 110840
ChinaSite Not Available

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