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Clinical efficacy and imaging evaluation of recombinant tissue plasminogen activator thrombolytic therapy in patients with wake up stroke:a randomized controlled trial

Clinical efficacy and imaging evaluation of recombinant tissue plasminogen activator thrombolytic therapy in patients with wake up stroke:a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034402
Enrollment
Unknown
Registered
2020-07-04
Start date
2021-02-01
Completion date
Unknown
Last updated
2020-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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Interventions

Experimental group:The treatment group was given rt-PA intravenous thrombolytic therapy (0.9 mg/kg, total amount <90 mg), and the brain CT was reviewed 24 hours later. Those without bleeding were give
Control group: The control group was given anti-platelet aggregation, lipid-lowering, stable plaque, blood circulation and other treatments.

Sponsors

Affiliated Hospital of North China University of Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Onset time: from the last seemingly normal state to symptom discovery 4.5 hours; 2. When the patient wakes up or is found by the witness, there is neurological deficit; 3. NIHSS score >=4; 4. Patients with no or early changes < 1 / 3 distribution area of middle cerebral artery; 5. Patients with mismatched DWI / FLAIR images (DWI developed but flair did not develop); 6. Patients who meet all other indications of intravenous thrombolysis; 7. Patients with large vessel occlusion should be treated with endovascular therapy. The treatment principle should refer to the consensus of Chinese experts on endovascular treatment of acute ischemic stroke.

Exclusion criteria

Exclusion criteria: 1. Patients with severe diseases such as malignant hypertension, severe arrhythmia, acute myocardial infarction, etc; 2. Patients with acute infection, trauma, surgery, diabetic ketoacidosis and hypertonic coma recently; 3. Patients with severe primary diseases such as liver, kidney and hematopoietic system; 4. Patients with tumor and other organ failure.

Design outcomes

Primary

MeasureTime frame
Neurological deficit score (NIHSS);Modified Rankin Scale (mRS) score;

Countries

China

Contacts

Public ContactChunyang Zhang

Affiliated Hospital of North China University of Technology

weykg0@163.com+86 315 3725358

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 17, 2026