Acute Ischemic Stroke Clinical Trial
Official title:
Feasibility and Efficacy of Intra- Arterial TNK and Albumin as an Adjunct to Thrombectomy for Acute Stroke
Verified date | October 2023 |
Source | Tianjin Huanhu Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to investigate the feasibility and efficacy of intra-arterial TNK and albumin for patients with acute ischemic stroke after successful thrombectomy and whether there is a synergistic effect between TNK and albumin.
Status | Recruiting |
Enrollment | 80 |
Est. completion date | September 7, 2024 |
Est. primary completion date | September 7, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion criteria: 1. AIS patients with large vessel occlusion; 2. Age between 18 and 80 years; 3. Baseline NIHSS score = 6; 4 .Successful recanalization after thrombectomy (mTICI grades = 2b); 5. ASPECTS score = 6 on CT; 6. First episode or previous episode without significant sequelae (mRS = 2); 7. Time from onset to femoral artery puncture = 24 hours; 8. Written informed consent provided by the patients or their legal relatives. Exclusion criteria: 1. Upon admission, the patient's medical history and physical examination revealed manifestations indicative of congestive heart failure (CHF), such as jugular venous distention, the presence of a third heart sound, resting tachycardia at a rate of 100 beats per minute attributable to heart failure, hepatomegaly, and/or lower extremity edema attributable to heart failure or of unknown etiology; 2. History of acute myocardial infarction within the preceding 3 months; 3. The patient's medical history, electrocardiogram findings upon admission, or physical examination indicated the presence of second- or third-degree heart block or any arrhythmia associated with hemodynamic instability, as determined by the investigator's assessment; 4. Acute or chronic renal failure with serum creatinine levels exceeding 2.0 mg/dL; 5. Severe anemia characterized by a hematocrit below 32%; 6. Computed tomography findings upon admission indicating the presence of any form of hemorrhage; 7. Pregnancy status; 8. Previous history of allergic reactions to albumin administration or TNK administration; 9. Elevated blood pressure exceeding 185/110 mmHg when investigating the use of albumin administration or TNK administration; 10. Presence of other potentially life-threatening medical conditions; 11. Individuals with current chronic lung diseases, such as chronic obstructive pulmonary disease, bronchiectasis, or any other lung disorder that significantly impairs daily activities; 12. Individuals with known allergies to albumin or TNK; 13. Patients with reocclusion within 24 hours; 14. Clinical suspicion of aortic coarctation? bacterial embolism and infective endocarditis; 15. Patients with a history of coagulation disorders and systemic bleeding tendencies. |
Country | Name | City | State |
---|---|---|---|
China | Tianjin Huanhu Hospital | Tianjin | Tianjin |
Lead Sponsor | Collaborator |
---|---|
Tianjin Huanhu Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of participants with major response | Major response is any of the following:
Any forms of intracranial hemorrhage; Pulmonary edema; Heart failure; Skin itching, dyspnea and other allergic reactions; Death of any causes. |
7 days after initiation of TNK or albumin intra-arterially |
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