Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 3:00 PM
Ignite Modification Date: 2025-12-24 @ 3:00 PM
NCT ID: NCT04581759
Eligibility Criteria: Inclusion Criteria: 1. acute ischemic stroke(AIS) patients with large vessel occlusion (internal carotid artery system and vertebral basilar artery system) within 24 hours after onset, endovascular treatment (mechanical thrombotomy, intra-arterial thrombolysis, balloon dilatation or stent angioplastyand) successful opening were performed, and the definition of successful opening was defined by Modified Thrombolysis standard \[Modified Thrombolysis in Cerebral infarction, mTICI\]≥ 2B,The standards of endovascular interventional treatment are in line with the indications and contraindications formulated in the Chinese Guidelines for the Early Treatment of Acute Ischemic Stroke 2018; 2. Modified Rankin scale score (mRS) ≤1 before onset: 3. The Alberta Stroke Program Early CT score (ASPECTS)≥6 on admission; 4. National Institute of Health Stroke Scale (NIHSS) score ≥6 on admission; 5. Provision of written informed consent. Exclusion Criteria: 1. CT or MRI scan showed significant midline deviation and the mass effect; 2. Glasgow(GCS) score ≤8 on admission; 3. failure to accomplish 3-months and 6-months follow up; 4. Severe cardiac, liver, or kidney disease, malignancy, severe coagulation dysfunction, severe anemia and systemic organ dysfunction; 5. Pregnant or nursing women, or patients with moderate to severe mental disorders or dementia; 6. Severe soft tissue injuries, fractures, thrombosis and other known peripheral vascular lesions of the upper limbs,active visceral hemorrhage, acute stage of fundus hemorrhage, cerebral aneurysm or cerebral arteriovenous malformation, and other unsuitable for bilateral upper arm compression.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT04581759
Study Brief:
Protocol Section: NCT04581759