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Starting soon Not applicable

Safety and Efficacy of Urinary Kallidinogenase for Large Artery Atherosclerosis Acute Ischemic Stroke

NCT06137300 · tracked via the Priya Life Science China tracker
Sponsor
Phase
Not applicable
Started
2024-03-15
Last updated
2024-02-28

Condition(s) studied

Acute Ischemic Stroke

Investigational drug(s) / intervention(s)

Urinary kallidinogenase for injection →Guideline-prescribed medical therapy

Urinary kallidinogenase for injection: Urinary kallidinogenase 0.15PNA once daily for 7 days.

Guideline-prescribed medical therapy: Guideline-prescribed medical therapy

Study summary

The purpose of this study is to evaluate the safety and efficacy of urinary kallidinogenase treatment in patients with large artery atherosclerotic acute ischemic stroke.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥18 years old; 2. Acute anterior circulation large artery atherosclerotic cerebral infarction (according to TOAST classification) within 48h of onset; NIHSS score ≥6, ≤15; 3. Moderate to severe stenosis or occlusion of offending vessels; 4. The mRS Score ≤2 before onset; 5. Subjects or their legal representatives agreed to the treatment and signed the informed consent form. Exclusion Criteria: 1. Transient ischemic attack; 2. Patients who planned or had received emergency reperfusion therapy (including intravenous thrombolysis and emergency thrombectomy); 3. Severe disturbance of consciousness:GCS ≤8; 4. Patients who previously received angiotensin-converting enzyme inhibitor (ACEI) drugs regularly; 5. Refractory hypertension: systolic blood pressure ≥200 mmHg or diastolic blood pressure ≥110 mmHg; hypotension: systolic blood pressure \< 90 mmHg or diastolic blood pressure \< 60 mmHg; 6. Liver dysfunction (ALT/AST \>1.5 × upper limit of normal \[ULN\]), renal dysfunction (Cr \>1 × ULN); 7. Coagulopathy (prolonged INR (\>1.5) or prolonged APTT (\>2 folds); 8. Cardioembolic stroke or high-risk factors of cardioembolic stroke identified by investigators (atrial fibrillation, cardiac mural thrombus, cardiomyopathy, etc.); 9. Special populations such as pregnant and lactating women, patients with life expectancy less than 3 months, or patients unable to complete the study for other reasons; 10. Unwilling to be followed up or poor treatment compliance; 11. Participating in other clinical investigators, or had participated in other clinical investigators within 3 months before enrollment; 12. Other conditions considered by the investigator to be inappropriate for enrollment.

Primary outcome measure(s)

  • Proportion of patients with Modified Rankin Scale (mRS) Score 0-2 at 90 days — 90 days
    Modified Rankin Scale (mRS) ranged from 0 to 6, a low value represents a better outcome.

Trial sites (1)

FacilityCityRegionStatus
First Hospital of Jilin University Changchun Jilin
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06137300 on ClinicalTrials.gov ↗ ← All trials in China