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Acute Ischemic Stroke EndoVascular Therapy: a Multicenter REGISTRY Study

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Naval Military Medical University

Status

Enrolling

Conditions

Thrombectomy
Large Vessel Occlusion
Thrombosis
Acute Ischemic Stroke

Treatments

Device: Endovascular treatment

Study type

Observational

Funder types

Other

Identifiers

NCT05864638
OCIN-AIS-EVT REGISTRY

Details and patient eligibility

About

A Multicenter Registry of Endovascular Treatment for Acute Ischemic Stroke.

Full description

The OCIN-AIS-EVT REGISTRY is a prospective, multicenter, blinded outcome evaluation, observational trial, and aims to determine the functional outcomes and safety of endovascular treatment for AIS, due to vessel occlusion in anterior and posterior circulation, in routine clinical practice.

The primary endpoint is functional outcome, defined as a shift (improvement) in scores on the modified Rankin scale (mRS) at 90 days (±7 days).

Enrollment

10,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Acute ischemic stroke caused by anterior or posterior circulation vessel occlusion confirmed by computed tomography angiography (CTA) or magnetic resonance angiography (MRA) or digital subtraction angiography (DSA)
  2. Undergo intravascular therapy (i.e. access to a cath lab and an arterial puncture)
  3. The patient or his/her legal representative agreed to participate in the study and has signed the informed consent.

Exclusion criteria

  1. No exclusion criteria

Trial design

10,000 participants in 1 patient group

Endovascular treatment
Treatment:
Device: Endovascular treatment

Trial contacts and locations

1

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Central trial contact

Pengfei Yang, M.D.

Data sourced from clinicaltrials.gov

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