Skip to content

Multicenter Prospective Observational Cohort Study of Symptomatic Atherosclerotic Non-acute Internal Carotid Artery Occlusion

Multicenter Prospective Observational Cohort Study of Symptomatic Atherosclerotic Non-acute Internal Carotid Artery Occlusion

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099580
Enrollment
Unknown
Registered
2025-03-26
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Symptomatic AtherosSymptomatic Non-acute Internal Carotid Artery Occlusion, SNICAO

Interventions

Observation Group:None

Sponsors

Yulin First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age> 18 years old; 2. Unilateral internal carotid artery occlusion detected by MRA/CTA/DSA; 3. The time from vascular occlusion to treatment is more than 24 hours (confirmed by imaging or inferred from the event of responsibility.; 4. Ipsilateral internal carotid artery occlusion related to liability events within the past 12 months, including ischemic stroke, TIA, or one or more of the transient monocular amaurosis (patients with only dizziness or headache are considered asymptomatic.; 5.mRS<=3; 6. Patients and their families are willing to participate in this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Occlusion caused by the following non-atherosclerotic diseases: such as arterial dissection, Takayasu's arteritis, moyamoya disease; vascular disease caused by herpes simplex virus, herpes zoster virus or other viruses; neurosyphilis; leptospira vasculitis; Any type of intracranial infection; radiation-induced vascular occlusion; fibromuscular dysplasia; sickle red cell anemia, etc.; 2. Previous history of primary intracranial or ventricular hemorrhage; 3. Active bleeding or known bleeding tendency within 30 days; 4. Cerebrovascular history of extracranial-intracranial vascular bypass grafting and/or occlusive vascular recanalization. 5. Patients with severe heart, liver, kidney, lung and other important organ diseases or functional failure; Those with tumors. 6. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
New stroke or death within 30 days after treatment;The incidence of composite endpoint events of ipsilateral ischemic stroke from 30 days to 2 years;

Secondary

MeasureTime frame
Symptomatic hemorrhage within 30 days after treatment;The incidence of all strokes at 3 months, 6 months, 12 months and 24 months after treatment;The incidence of all deaths at 3 months, 6 months, 12 months and 24 months after treatment;The incidence of all strokes and deaths at 3 months, 6 months, 12 months and 24 months after treatment;The mRS scores at 3 months, 6 months, 12 months and 24 months after treatment;

Countries

China

Contacts

Public ContactLin Yanni

Yulin First People's Hospital

ylssjnk@126.com+86 186 0775 5618

Outcome results

None listed

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