Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT07509645

Efficacy and Safety of Interleukin-6 Receptor Inhibitor Combined With Endovascular Treatment in Patients With Acute Posterior Circulation Large Vessel Occlusion Stroke

Led by Capital Medical University · Updated on 2026-05-05

348

Participants Needed

13

Research Sites

51 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is an investigator-initiated phase III clinical trial employing a randomized, double-blind, placebo-controlled design. The primary objective of this study is to investigate the efficacy and safety of an interleukin-6 inhibitor (tocilizumab) combined with endovascular therapy in patients with acute posterior circulation large-vessel occlusion stroke.

CONDITIONS

Official Title

Efficacy and Safety of Interleukin-6 Receptor Inhibitor Combined With Endovascular Treatment in Patients With Acute Posterior Circulation Large Vessel Occlusion Stroke

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older, any gender
  • Acute ischemic stroke caused by basilar artery occlusion
  • Planned emergency endovascular treatment
  • Time from stroke onset to groin puncture within 24 hours
  • National Institutes of Health Stroke Scale (NIHSS) score of 10 or higher
  • Posterior circulation Alberta Stroke Program Early CT score (pc-ASPECTS) of 6 or higher
  • Signed informed consent from patient or legally authorized representative
Not Eligible

You will not qualify if you...

  • Presence of intracerebral hemorrhage, epidural hematoma, subdural hematoma, intraventricular hemorrhage, or subarachnoid hemorrhage
  • Pre-stroke modified Rankin scale (mRS) score greater than 1
  • Known allergy to tocilizumab or excipients
  • Known allergy to iodinated contrast agents
  • Difficulty completing endovascular treatment due to vascular tortuosity
  • History of bleeding disorders, coagulation factor deficiencies, or thrombocytopenic diseases
  • Systolic blood pressure 180 mmHg or higher or diastolic blood pressure 110 mmHg or higher despite control
  • Neutrophil count less than 2 x 10^9 /L
  • Platelet count less than 100 x 10^9 /L
  • Blood glucose less than 2.8 mmol/L (50 mg/dL) or greater than 22.2 mmol/L (400 mg/dL)
  • Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels more than twice the upper limit of normal
  • Recent or current serum creatinine more than twice the upper limit of normal or estimated glomerular filtration rate (eGFR) less than 60 mL/min
  • Pregnant, lactating, or planning pregnancy within 90 days
  • Severe mental disorders or inability to comply with consent and follow-up due to dementia
  • Concurrent malignant tumors or severe systemic diseases with expected survival less than 90 days
  • Presence of autoimmune diseases or use of immunosuppressive drugs
  • Systemic infectious diseases
  • Participation in another interventional clinical trial within 30 days before randomization or currently participating in another interventional trial
  • Any condition judged by investigators to pose harm if study therapy is initiated
  • Other conditions that may affect compliance or preclude participation as assessed by the investigator

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 13 locations

1

Suzhou Municipal Hospital

Suzhou, Anhui, China, 234000

Actively Recruiting

2

Anyang People's Hospital

Anyang, Henan, China, 455000

Actively Recruiting

3

Nanyang Central Hospital

Nanyang, Henan, China, 473000

Actively Recruiting

4

The First Affiliated Hospital of Henan Medical University

Xinxiang, Henan, China, 453000

Actively Recruiting

5

People's Hospital of Xihua

Zhoukou, Henan, China, 466600

Actively Recruiting

6

People's Hospital of Linyi

Linyi, Shandong, China, 276000

Actively Recruiting

7

Zibo Central Hospital

Zibo, Shandong, China, 255000

Actively Recruiting

8

Xianyang First People's Hospital

Xianyang, Shanxi, China, 712000

Actively Recruiting

9

Yuncheng Central Hospital

Yuncheng, Shanxi, China, 044000

Actively Recruiting

10

Lishui Central Hospital

Lishui, Zhejiang, China, 323000

Actively Recruiting

11

Taizhou enze Hospital

Taizhou, Zhejiang, China, 318000

Actively Recruiting

12

People's Hospital of Yueqing

Yueqing, Zhejiang, China, 325600

Actively Recruiting

13

Capital Medical Univercity Xuanwu Hospital

Beijing, China, 100053

Actively Recruiting

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Research Team

X

Xunming Ji

CONTACT

C

Chuanjie Wu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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