Safety and Efficacy of Remote Ischemic Conditioning in Patients With Severe Stenosis or Occlusion of Anterior Intracranial Circulation Vessels (RICASO)

University of Science and Technology of China (USTC)

Status: Terminated

Conditions: Acute Ischemic Stroke

Treatments: Device: RIC; Other: Guideline-based therapy; Device: Sham

Study type: Interventional

Funder types: Other

Identifiers

NCT06823128

RICASO

Details and patient eligibility

About

The primary purpose of this study is to examine whether remote ischemic treatment can better the 90 - day neurological outcomes in acute ischemic stroke patients having severe stenosis or occlusion of anterior intracranial circulation vessels.

Enrollment: 458 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age is 18 years old or above.
2. Severe stenosis (70% - 99%) or occlusion of anterior intracranial circulation vessels, mainly including the intracranial segment of the internal carotid artery, middle cerebral artery (M1, M2) and anterior cerebral artery (A1, A2), which is confirmed by digital subtraction angiography (DSA), computed tomography angiography (CTA) or magnetic resonance angiography (MRA).
3. Patients with clinically diagnosed acute ischemic stroke who received remote ischemic treatment within 72 hours after the onset.
4. The NIHSS score ranges from 4 to 24.
5. The mRS score before stroke is less than or equal to 1.
6. informed consent.

Exclusion criteria

1. Patients with vessel recanalization after mechanical thrombectomy (TICI grade ≥ 2b).
2. Patients planning to receive intracranial endovascular treatment within 3 months.
3. Patients diagnosed with acute posterior circulation cerebral infarction.
4. Symptoms caused by non - culprit vessels.
5. Ipsilateral extracranial vessel stenosis ≥ 70%.
6. Systolic blood pressure > 185 mmHg or diastolic blood pressure > 110 mmHg, and uncontrollable by antihypertensive drugs.
7. Intracranial tumors, arteriovenous malformations or aneurysms.
8. Cerebral venous thrombosis or stenosis.
9. Severe coagulation abnormalities.
10. Any contraindications to remote ischemic conditioning: severe soft tissue injury, fracture or vascular injury of the upper limb, perivascular lesions of the distal upper limb, etc.
11. Patients with any serious diseases and a life expectancy of less than 1 year.
12. Patients who participated in other clinical trials within 3 months before enrollment or are currently participating in other clinical trials.
13. Patients who cannot be followed up (such as those without a fixed residence, overseas patients, etc.).
14. Pregnant or lactating women.
15. Patients who have previously received remote ischemic treatment or similar treatments.
16. Patients whom the researchers consider unsuitable for this clinical study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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458 participants in 2 patient groups

RIC group+Guideline-based therapy

Experimental group

Description:

RIC is given twice a day with 200mmHg pressure.

Treatment:

Other: Guideline-based therapy

Device: RIC

Sham group+Guideline-based therapy

Active Comparator group

Description:

RIC is given twice a day with 60mmHg pressure.

Treatment:

Device: Sham

Other: Guideline-based therapy