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A multicenter, randomized, controlled clinical trial of endovascular treatment for acute basilar artery occlusion 2

A multicenter, randomized, controlled clinical trial of endovascular treatment for acute basilar artery occlusion 2

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040902
Enrollment
Unknown
Registered
2020-12-14
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-05-10

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

Conditions

Acute posterior circulation large vessel occlusion

Interventions

EVT combined with SMT group:EVT combined with SMT
standard medicine treatment group:SMT

Sponsors

The Second Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Preliminarily judged as posterior circulation ischemic stroke based on clinical symptoms or imaging examination; 2) Posterior circulation aorta occlusion confirmed by CTA/MRA/DSA (basal artery and isolated vertebral artery V4 segment); 3) Aged 18-80 years; 4) The time from onset to randomization is within 24 hours; 5) NIHSS score >= 10 points; 6) PC-ASPECT score >= 6 points; 7) Patient or family members sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Cerebral CT or MRI confirmed intracranial hemorrhage; 2) mRS score >= 3 points before the onset; 3) Pregnant or breastfeeding women; 4) Allergy to contrast agents or nickel-titanium alloy; 5) Participating in other clinical trials; 6) Contraction Pressure> 185 mmHg or diastolic blood pressure> 110 mmHg, and oral antihypertensive drugs cannot be controlled; 7) Genetics or acquired hemorrhage, lack of anticoagulant factors; or oral anticoagulants and INR>1.7; 8) Blood glucose 400 mg/dl (22.2 mmol/L), platelets <100*10^9/L, or hematocrit <25%; 9) The artery is tortuous until the thrombus removal device cannot reach the target blood vessel; 10) Hemorrhage history in the past 6 months; 11) Life expectancy <1 year; 12) Expected failure to complete follow-up; 13) Obvious mass effect or hydrocephalus in the cerebellar hemisphere on imaging; 14) Bilateral brain on imaging Diffuse ischemic manifestations.

Design outcomes

Primary

MeasureTime frame
mRS in 0-3 score at 90 days;The incidence of symptomatic intracranial hemorrhage within 48 hours and the 90-day mortality rate.;

Secondary

MeasureTime frame
Changes in NIHSS score 5-7 days after operation;Changes in NIHSS score 24h after operation;Incidence of complications of non-intracranial hemorrhage;Operation and device-related complications.;

Countries

China

Contacts

Public ContactQingwu Yang

The Second Affiliated Hospital of the Army Medical University

yangqwmlys@163.com+86 13657638868

Outcome results

None listed

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