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Chinese Cohort of Tenecteplase Thrombolysis for Acute Ischemic Stroke

Chinese Cohort of Tenecteplase Thrombolysis for Acute Ischemic Stroke((CREAT-TNK Study)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091196
Enrollment
Unknown
Registered
2024-10-23
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

Lschemic stroke

Interventions

Standard medical therapy and tenecteplase group:NA

Sponsors

Second Affiliated Hospital of Army Medical University, PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age =18 years; 2) Preliminary diagnosis of acute ischemic stroke according to clinical symptoms and signs; 3) Acute ischemic stroke confirmed by CT/MRI; 4) Thrombolysis with tenecteplase; 5) Patients or their family members provided written informed consent.

Exclusion criteria

Exclusion criteria: 1) Intracranial hemorrhage confirmed by head CT or MRI; 2) Expected inability to complete follow-up; 3) Patients who were deemed unsuitable for study participation by the investigator; 4) Active internal bleeding; 5) Significant bleeding illness currently or in the past 6 months; 6) Known or suspected history of intracranial hemorrhage; 7) Known bleeding constitution; 8) Significant or recent severe or dangerous bleeding; 9) A history of central nervous system disease or trauma (e.g., intracranial tumor, arteriovenous malformation or aneurysm, intracranial or intraspinal surgery); 10) Aneurysmal subarachnoid hemorrhage or suspected subarachnoid hemorrhage; 11) Tumors with a tendency to bleed; 12) Bacterial endocarditis or pericarditis; 13) A recent (within 2 weeks) prolonged (>2 minutes) cardiopulmonary resuscitation, delivery, or nonpressure vessel puncture (e.g., subclavian or jugular venepuncture); 14) Acute pancreatitis, active gastrointestinal ulcer, aneurysm or arterial/venous malformation; 15) Oral anticoagulant therapy and INR>1.3; 16) Severe liver disease, including liver failure, cirrhosis, portal hypertension (esophageal varices), and active hepatitis; 17) Severe trauma or major surgery in the past 3 months.

Design outcomes

Primary

MeasureTime frame
90-day mRS Score;Incidence of symptomatic intracranial hemorrhage;90-day mortality;

Secondary

MeasureTime frame
The proportion of 90-day mRS Scores 0-2;The proportion of 90-day mRS Scores 0-1;Changes of NIHSS score 5-7 days after surgery;90-day EQ-5D scale score;incidence of asymptomatic intracranial hemorrhage;Incidence of non-intracranial hemorrhage complications;Incidence of non-hemorrhagic serious adverse events;

Countries

China

Contacts

Public ContactWenjie Zi

Second Affiliated Hospital of Army Medical University, PLA

Ziwenjie1981@163.com+86 182 0519 2720

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026