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Multi-center observational study of endovascular recanalization in acute ischemic stroke

Multi-center prospective registry study for endovascular treatment of acute ischemic stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-17013052
Enrollment
Unknown
Registered
2017-10-20
Start date
2017-03-08
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

Acute Ischemic Stroke

Interventions

After intravenous thrombolysis bridging endovascular therapy group :N/A
Direct endovascular therapy group:N/A

Sponsors

the First Affiliated Hospital of Jinan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) aged= 18 years old; 2) were confirmed by stroke diagnosis standard in 1994 fourth national cerebrovascular disease conference to determine the examination,combine with clinical symptoms and imaging; 3) onset time= 24 hours; 4)underwent endovascular treatment; 4) patients / families get the informed consent for the study.

Exclusion criteria

Exclusion criteria: 1) those who had mental illness or cognitive impairment and could not live normally; 2) important organs with serious diseases; 3) refused to participate in the study; 4) other patients who were not suitable for the study.

Design outcomes

Primary

MeasureTime frame
Pre stroke mRS;Preoperative mRS after stroke;Toast type;Main responsible vessels;Stroke onset to admission time;Door to Needle time(DNT);From door to groin puncture;Time from puncture to recanalization;Baseline NIHSS score;NIHSS score within 24h;NIHSS score within 7 days;postoperative mTICI;Way of endovascular treatment;Stent thrombectomy;balloon dilatation;balloon dilatation;Intra-arterial thrombolysis;Tirofiban perfusion therapy;Operation complication;symptomatic ICH;death;mRS at 90 days;mRS at 12 months;Recurrent ischemic stroke within 90 days;Recurrent ischemic stroke within 12 months;

Secondary

MeasureTime frame
Age;Sex;BMI;Smoking history;Hypertension history;Diabetic history;Atrial fibrillation history;History of coronary heart disease;History of heart valve disease;Stroke history;History of peripheral vascular disease;History of antiplatelet agents;Oral anticoagulant history;Antihypertensive drug history;Systolic blood pressure at admission;Diastolic blood pressure at admission;First fasting blood glucose at admission;INR value at admission;First platelet count;First total cholesterol value;First triglyceride value;Preoperative CT-ASPECT score;Preoperative DWI-ASPECT score;anesthesia methods;Preoperative mTICI;

Countries

China

Contacts

Public ContactLi'an Huang

the First Affiliated Hospital of Jinan University

huanglian1306@126.com+86 20-38688637

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026