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Prospective multicenter registry study of recanalization treatment of nonacute cerebral artery occlusion in ischemic stroke

Prospective multicenter registry study of recanalization treatment of nonacute cerebral artery occlusion in ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OON-17011419
Enrollment
Unknown
Registered
2017-05-17
Start date
2017-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Cerebral artery occlusion

Interventions

Interventional recanalization group:Interventional recanalization
Hybrid surgery group:Hybrid surgery

Sponsors

Henan Provincial People' Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Age 30-90 years old; 2. Detection of non-acute large cerebral artery occlusion (TICI grade 0); 3. Cerebral artery occlusion for more than 24 hours (imaging confirmed, or inferred from the responsibility ischemic events); 4. Ischemic responsibility events are associated with occlusive cerebral artery (including Stroke, TIA); 5. mRS scale score =4; 6. Patients are willing to go to the institution or the physician of this study for the regular follow-up; 7. Patients and their families can conduct telephone follow-up; 8. Patients could understand the meaning and purpose of this study and sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Stroke of the lesion with a maximum diameter of = 5cm or transverse to the midbrain or pons 3/4; 2. Any hemorrhagic stroke within 14 days; 3. Simultaneous detection of more than two large vessels of non-acute occlusion, and can not determine the responsibility of blood vessels; 4. Occlusion of blood vessels near the heart or distal end of any residual vascular diameter = 1.5mm; 5. Occlusion caused by the following non-atherosclerotic diseases such as arterial dissection, Takayasu's disease, moyamoya; herpes simplex virus, herpes zoster virus or other virus-induced vascular disease; neurosyphilis; leptospira Vasculitis; any type of intracranial infection; radiation-induced vascular occlusion; fibromuscular dysplasia; sickle red blood cell anemia; 6. Within 30 days of any intracranial hemorrhage (including subarachnoid hemorrhage, subdural or epidural hemorrhage); 7. Have had the primary intracranial or ventricular hemorrhage 8. Within 30 days before or within 90 days of major surgery (including femoral artery, aorta or carotid artery surgery); 9. Activated gastrointestinal ulcers, 30 days of systemic bleeding, active bloody diarrhea, platelet count 1.5, coagulation factor abnormalities lead to increased risk of bleeding; 10. Severe liver damage (ALT or AST> normal upper limit 3 times, cirrhosis), creatinine> 3.0 (unless the patient is dialysis); combined heart, respiratory failure; 11. Clearly allergic or contraindicated to aspirin, clopidogrel, heparin, stent component nickel-titanium alloy and local anesthetic or general anesthetic; 12. On the contrast agent has a history of fatal allergies; if allergic but not fatal, can be preoperative by the specialist carefully assessed after the effective prevention; 13. Life expectancy of no more than 3 years; and combined intracranial or extracranial malignant tumors; Combined with malignant tumors; with the heart, liver, kidney, lung and other vital organs or functional failure; 14. Other studies that have been included may be in conflict with current research.

Design outcomes

Primary

MeasureTime frame
Stroke;

Countries

China

Contacts

Public ContactTianxiao Li

Henan Provincial People's Hospital

dr.litianxiao@vip.163.com+86 18603869791

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026