Skip to content

The efficacy and safety of endovascular recanalization for symptomatic chronic occlusion of the internal carotid artery: a prospective, multicenter registry study

The efficacy and safety of endovascular recanalization for symptomatic chronic occlusion of the internal carotid artery: a prospective, multicenter registry study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114386
Enrollment
Unknown
Registered
2025-12-11
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Symptomatic chronic occlusion of intracranial arteries in patients

Interventions

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age greater than 18 years; 2. CT angiography or magnetic resonance angiography shows 100% occlusion of the cross-sectional area of the intracranial arteries; 3. The occlusion time is more than 4 weeks from the discovery to the present (confirmed by imaging, or inferred based on the responsible event); 4. Any of the following clinical symptoms occur: (1) ischemic stroke; (2) recurrent dizziness, discomfort, and sluggishness due to hypoperfusion; (3) transient blindness symptoms occur; (4) mild cognitive dysfunction; 5. The patient or legal representative signs a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Imaging confirmed intracranial hemorrhage; 2. mRS score >= 3 points; 3. Complicated with severe intracranial artery stenosis in the posterior circulation; 4. Pregnant or lactating women; 5. Severe dementia (MOCA score 1.5, increased bleeding risk due to abnormal coagulation factors; 9. Severe liver damage (ALT or AST > three times the upper limit of normal, liver cirrhosis), creatinine > 3.0 mg/dl (unless the patient is on dialysis); patients with combined heart or respiratory system failure; 10. Allergic or contraindicated to aspirin, clopidogrel, heparin, nickel-titanium alloy of stent components, local anesthetic or general anesthetic drugs; 11. Fatal allergy to contrast agents; if allergic but not fatal, it can be effectively prevented after careful assessment by a specialist before the operation; 12. Those with an expected survival of no more than 3 years, or those with concomitant intracranial or extracranial malignant tumors; 13. Already enrolled in other studies that may conflict with the current study; 14. Expected not to be able to complete follow-up.

Design outcomes

Primary

MeasureTime frame
Any stroke event or death within 30 days after enrollment;Within 30 days to 1 year after enrollment, ischemic stroke events in the area supplied by the responsible blood vessel;

Secondary

MeasureTime frame
Neurological function assessment (mRS score) 90 days after enrollment;The incidence rates of hemorrhagic stroke, ischemic stroke and death within 30 days after enrollment;The incidence of ischemic stroke in the area supplied by the responsible blood vessels within one year after enrollment;Neurological function assessment (mRS score) one year after enrollment;All-cause mortality within one year after enrollment;The incidence of symptomatic cerebral hemorrhage within one year after enrollment;Rate of recanalization of occluded blood vessels within 1 year;One-year cognitive function;

Countries

China

Contacts

Public ContactYangmei Chen

The Second Affiliated Hospital of Chongqing Medical University

chenym1997@sina.com+86 136 0834 8562

Outcome results

None listed

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