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To establish and validate a predictive model for reperfusion failure and critical complications in patients with acute ischemic stroke

To establish and validate a predictive model for reperfusion failure and critical complications in patients with acute ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099126
Enrollment
Unknown
Registered
2025-03-18
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Acute ischemic stroke

Interventions

Observation group:None

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age>=18 years old; 2. Preliminary judgment of acute ischemic stroke according to clinical symptoms and signs; 3. Imaging CT/MRI confirmed as acute ischemic stroke; 4. Receiving reperfusion therapy; 5. Signed written informed consent by the patient or family member.

Exclusion criteria

Exclusion criteria: 1.Intracranial hemorrhage confirmed by cranial CT or MRI; 2.Expected to be unable to complete the follow - up; 3.Patients deemed unsuitable for participation by the researchers; 4.Active internal hemorrhage; 5.Have had obvious hemorrhagic diseases currently or in the past 6 months; 6.Known history of intracranial hemorrhage or suspected intracranial hemorrhage; 7.Known bleeding diathesis; 8.Significant or recent severe or dangerous bleeding; 9.Central nervous system lesions or trauma history (such as intracranial tumors, arteriovenous malformations or aneurysms, intracranial or intraspinal surgery); 10.Aneurysmal subarachnoid hemorrhage or suspected subarachnoid hemorrhage; 11.Tumors with a bleeding tendency; 12.Bacterial endocarditis or pericarditis; 13.Have undergone cardiopulmonary resuscitation for a long time (> 2 minutes), childbirth or non - pressure vascular puncture (such as subclavian or jugular vein puncture) within the last 2 weeks; 14.Acute pancreatitis, active peptic ulcer, aneurysm or arteriovenous malformation. 15.Taking oral anticoagulant therapy with an INR > 1.3; 16.Severe liver diseases, including liver failure, cirrhosis, portal hypertension (esophageal varices) and active hepatitis; 17.Have had severe trauma or major surgery in the past 3 months.

Design outcomes

Primary

MeasureTime frame
Modified Rankin Scale Score;Incidence of symptomatic intracranial hemorrhage (SICH) within 48 hours after completion of tirofiban treatment and 90-day mortality;

Secondary

MeasureTime frame
National Institute of Health Stroke Scale Score;EuroQol Five Dimensions Questionnaire Score;Incidence of asymptomatic intracranial hemorrhage (aSICH) within 48 hours;Incidence of non-intracranial bleeding complications (including gastrointestinal bleeding, urethral bleeding, oral or nasal mucosal bleeding, and subcutaneous hematoma);Incidence of non-hemorrhagic serious adverse events;

Countries

China

Contacts

Public ContactHu Bo

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

hubo@mail.hust.edu.cn+86 13707114863

Outcome results

None listed

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