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Study on early reperfusion therapy Strategy and related mechanisms for Intracranial artery severe stenosis or occlusive stroke

Study on early reperfusion therapy Strategy and related mechanisms for Intracranial artery severe stenosis or occlusive stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124212
Enrollment
Unknown
Registered
2026-05-08
Start date
2023-09-16
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

intracranial artery severe stenosis or occlusive acute ischemic stroke

Interventions

Interventional therapy group for mild stroke:None
Drug treatment group for mild stroke:None
Moderate-severe stroke:None

Sponsors

Yongchuan Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age = 18 years; 2. The time from the onset of the first stroke symptom to admission is within 72 hours; 3. Judged as acute anterior circulation ischemic stroke based on clinical manifestations and imaging examinations; 4. CTA/MRA/DSA confirmed that the responsible vessel is the C6-7 segment of ICA, M1, M2, A1, A2, A3 with severe stenosis (stenosis rate = 70%, stenosis rate = (1 - D stenosis / D normal) × 100%, where D stenosis refers to the diameter of the most severely stenotic part of the artery, and D normal refers to the diameter of the normal artery at the proximal end of the stenosis); 5. The patient or the patient's family signed a written informed consent form.

Exclusion criteria

Exclusion criteria: 1.Intracranial hemorrhagic diseases confirmed by CT or MRI; 2. midline shift shown by CT or MRI; 3. chronic occlusion or dissection of the responsible vessel confirmed or suspected clinically; 4.mRS = 2 before the onset; 5. pregnant or lactating women; 6.severe renal dysfunction (serum creatinine > 220 µmol/L); 7.iodine contrast agent allergy; 8.high bleeding risk (platelet count 50 seconds or PT-INR > 3.0), or existing coagulation disorders, history of systemic bleeding; 9.severe or fatal comorbidities (hepatic and renal dysfunction, cardiac and pulmonary dysfunction, expected survival time less than 6 months, etc.); 10.the investigator judges that endovascular treatment is not suitable; 11.due to various reasons such as mental disorders, cognitive or emotional disorders, the investigator judges that the subject is likely to have poor compliance.

Design outcomes

Primary

MeasureTime frame
Modified Rankin scale score 90 days after oneset;Mortality at 90 days after interventional therapy;Other procedure-related complications;The vessel was reoccluded within 7 days after interventional therapy;Symptomatic intracranial hemorrhage (The National Institutes of Health Stroke Scale increase =4) within 48 hours after surgery;Recurrent ischemic stroke within 90 days;the success rate of interventional therapy group;Any intracranial hemorrhage within 48 hours;

Secondary

MeasureTime frame
The NIHSS score improved by =4 points within 48 hours after interventional therapy;percentage of patients with a modified Rankin scale score of 0-1 at 90 days after oneset;percentage of patients with a modified Rankin scale score of 0-1 at 90 days after oneset;

Countries

China

Contacts

Public ContactGao xiangjie

Yongchuan Hospital of Chongqing Medical University

747736553@qq.com+86 136 5835 8637

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026