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Intravenous ThrombolysisRegistry for Acute Ischemic Stroke

Intravenous ThrombolysisRegistry for Acute Ischemic Stroke

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-17013788
Enrollment
Unknown
Registered
2017-12-08
Start date
2018-01-01
Completion date
Unknown
Last updated
2017-12-11

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

Conditions

Acute Ischemic Stroke

Interventions

UK:1.2 million U or 1.5 million U dissolved in 100ml sodium chloride injection, 30 minutes intravenously finished
rtpa:According to 0.6mg / kg or 0.9mg / kg alteplase, of which 10% intravenous injection, the remaining 60 minutes intravenous infusion

Sponsors

The General Hospital of Shenyang Military Region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) aged =18 years; 2) meet the diagnostic criteria for the diagnosis and treatment of acute ischemic stroke in China 2014; 3) the first onset or previous history of cerebral infarction without significant sequelae (mRS = 1); 4) within 6 hours of onset; 5) Patients or legal guardians are able to understand and sign informed consent.

Exclusion criteria

Exclusion criteria: Absolute exclusion criteria: 1. Significant history of head trauma or stroke in the last 3 months; 2. Suspected subarachnoid hemorrhage; 3. History of previous intracranial hemorrhage; 4. Intracranial neoplasms, arteriovenous malformations or aneurysms; 5. intracranial or spinal surgery in the near future; 6. arterial puncture in the last 7 days; 7. elevated blood pressure: systolic blood pressure =180 mm Hg, or diastolic blood pressure = 100 mm Hg; 8. activity; 9. acute bleeding tendency, including platelet count less than 100×10^9/L or other conditions; 10. received heparin treatment within 48 h (APTT exceeded the upper limit of normal range); 11. oral anticoagulant, INR> 1.7 Or PT> 15S; 12. are currently using thrombin inhibitors or Xa factor inhibitors, various sensitive laboratory tests (eg APTT, INR, platelet count, ECT; TT or appropriate Xa factor activity assay); 13. Blood glucose 1/3 cerebral hemisphere); 15. Researchers are not considered eligible for other clinical studies; 16. within 3 months or are participating in other clinical trials; 17. combined with severe systemic systemic disease is expected to survive less than three months: 1) severe stroke (NIHSS> 25 points); 2) pregnancy; 3) residual neurological deficits after epileptic seizures; 4) major surgery or severe trauma in the last 14 days; 5) Urethral bleeding; 6) myocardial infarction in the last 3 months.

Design outcomes

Primary

MeasureTime frame
mRS;

Secondary

MeasureTime frame
NIHSS;Recurrent Stroke;

Countries

China

Contacts

Public ContactHuisheng Chen

The General Hospital of Shenyang Military Region

chszh@aliyun.com+86 13352452086

Outcome results

None listed

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