Actively Recruiting
Acute Ischemic Stroke EndoVascular Therapy: a Multicenter REGISTRY Study (OCIN-AIS-EVT REGISTRY)
Led by Changhai Hospital · Updated on 2025-01-27
10000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to observe and evaluate the outcomes of endovascular treatment for acute ischemic stroke (AIS) caused by vessel blockage in the brain's anterior or posterior circulation. The study is a prospective, multicenter, observational trial designed to assess the safety and functional recovery of patients receiving this treatment in routine clinical settings. Participants receive endovascular treatment, which may include mechanical thrombectomy using devices such as stents, aspiration catheters, or combinations with intra-arterial clot-dissolving therapies. The study records these procedures as part of standard care without randomization or comparison groups since it is observational. During the study, researchers will track patients' recovery and safety outcomes through various assessments, including a primary focus on functional improvement measured by the modified Rankin scale at 90 days. Additional measures include neurological status at 24 hours and 7 days, as well as details about blood vessel reopening immediately after and during the procedure. The study intends to provide insights into real-world treatment results and safety over the follow-up period.
CONDITIONS
Brief Title
Acute Ischemic Stroke EndoVascular Therapy: a Multicenter REGISTRY Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Acute ischemic stroke caused by vessel blockage in anterior or posterior circulation confirmed by CTA, MRA, or DSA
- Undergoing intravascular therapy with arterial access
- Patient or legal representative has agreed to participate and signed informed consent
You will not qualify if you...
- No exclusion criteria
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 day
Participants undergo endovascular treatment such as mechanical thrombectomy for acute ischemic stroke.
1 procedure visit
Duration - 90 days
Participants are monitored to assess functional outcomes and safety following the endovascular treatment.
Visits at 24 hours, 7 days, and 90 days post-procedure
Trial Site Locations
Total: 1 location
1
Jianimin Liu
Shanghai, China
Actively Recruiting
Research Team
P
Pengfei Yang, M.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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