RecruitingPhase 3NCT07263308

Albumin for Patients With Acute Large Vessel Occlusive Stroke Undergoing Endovascular Therapy -2


Sponsor

Capital Medical University

Enrollment

1,192 participants

Start Date

Dec 18, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study is a prospective, multicenter, open-label, randomized controlled clinical trial. The investigators will apply albumin to the reperfusion treatment of patients with acute ischemic stroke in the anterior circulation. This study aims to verify the efficacy and safety of albumin combined with endovascular treatment in patients with anterior circulation acute ischemic stroke.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria7

  • Age between 18 and 80 years;
  • Acute ischemic stroke with indications for endovascular treatment within 24 hours of onset;
  • Anterior circulation acute ischemic stroke, with acute occlusion of the responsible vessel located in the intracranial segment of the internal carotid artery, or the M1 or M2 segment of the middle cerebral artery;
  • National Institute of Health Stroke Scale (NIHSS) score >=6;
  • Alberta Stroke Program Early CT Score (ASPECTS) >=3 points;
  • Modified Rankin Scale (mRS) score ≤1 before onset of the disease;
  • Written informed consent provided by the patients or their legal relatives.

Exclusion Criteria23

  • Evidence of intracranial hemorrhage (intracerebral hematoma (ICH), subarachnoid hemorrhage (SAH), epidural hemorrhage, acute or chronic subdural hematoma (SDH)) on the baseline CT or MRI scan;
  • History of congenital or acquired bleeding disorders, coagulation factor deficiency diseases, thrombocytopenic diseases, etc;
  • Anticipated difficulty in completing endovascular treatment due to vascular tortuosity;
  • Known severe allergy (more severe than skin rash) to contrast agents uncontrolled by medications;
  • Pregnancy, breastfeeding;
  • An episode or exacerbation of congestive heart failure from any cause in the past 6 months;
  • History of heart valve disease complicated by congestive heart failure within the past 6 months;
  • Cardiac surgery with thoracotomy (eg. coronary artery bypass grafting or valve replacement surgery) within the past 6 months;
  • Acute myocardial infarction in the past 6 months;
  • Signs or symptoms of acute myocardial infarction upon admission, including electrocardiographic findings;
  • Elevated serum troponin concentration upon admission (>0.1 μg/L) ;
  • Acute arrhythmia (including any tachycardia or bradycardia) with hemodynamic instability (systolic blood pressure <100 mm Hg) upon admission;
  • Acute or chronic lung diseases requiring long-term or intermittent oxygen therapy;
  • Findings on physical examination of any of the following abnormalities: (1) Jugular venous distension (jugular venous pulsation >4 cm above the sternal angle); (2) Resting tachycardia due to congestive heart failure (heart rate > 100 per/min); (3) Third heart sound; (4) Abnormal hepatic jugular venous reflux; (5) Pitting edema of the lower extremities attributable to congestive heart failure or without apparent cause; (6) Rales in both lungs; (7) Or evidence of pulmonary edema, pleural effusion, or pulmonary vascular redistribution on chest X-ray;
  • Severe chronic anemia (hemoglobin < 75 g/L);
  • Known recent or current serum creatinine exceeding 1.5 times the upper limit of normal, or estimated glomerular filtration rate (eGFR) < 60 mL/min;
  • Refractory hypertension that is difficult to control by medication (defined as systolic blood pressure > 220 mmHg, or diastolic blood pressure > 110 mmHg);
  • Serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) is greater than 1.5 times the upper limit of the normal value.
  • History of albumin allergy or known allergy to albumin;
  • Patients with severe mental disorders or dementia who are unable to cooperate in completing informed consent and follow-up content;
  • The expected survival time is less than 90 days (such as comorbidity with malignant tumor or severe systemic diseases etc.);
  • Patients who have participated in other interventional clinical studies within 30 days before randomization or are currently participating in other interventional clinical studies.
  • The investigator believes that the subject has other conditions making it unsuitable for participating in this study.

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Interventions

DRUGAlbumin

25% human albumin at a dose of 0.5g/kg (maximum dose 37.5g) should be administered intravenously. On the second, third, and fourth days, 25% human albumin at a dose of 0.5g/kg (maximum dose 37.5g) should be administered daily.

PROCEDUREEndovascular treatment

Best endovascular treatment.


Locations(12)

Taihe County Hospital of Traditional Chinese Medicine

Fuyang, Anhui, China

Si County People's Hospital

Suzhou, Anhui, China

Xuanwu Hospital,Capital Medical University

Beijing, Beijing Municipality, China

Shanghai General Hospital Jiujuan Hospital

Jiuquan, Gansu, China

Gansu Provincial Hospital

Lanzhou, Gansu, China

Jixi People's Hospital

Jixi, Heilongjiang, China

Ningling County People's Hospital

Shangqiu, Henan, China

The First Affiliated Hospital of Xinxiang Medical University

Weihui, Henan, China

The First Affiliated Hospital of Henan University of Chinese Medicine

Zhengzhou, Henan, China

Zhongmou County People's Hospital

Zhengzhou, Henan, China

Rizhao Hospital of Traditional Chinese Medicine

Rizhao, Shandong, China

Laizhou People's Hospital

Yantai, Shandong, China

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NCT07263308


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