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Remote Ischemic Conditioning Tested for Acute Moderate Stroke From Artery Narrowing

Tests remote ischemic conditioning, applied with a device, in adults with acute moderate stroke.

Key facts

Who runs it
First Affiliated Hospital Xi'an Jiaotong University
Where
Xi’an, ChinaSee the site
Trial code
Registry title
Remote Ischemic Conditioning for Acute Moderate Ischemic Stroke Due to Large Artery Atherosclerosis
Status
Recruiting
People taking part
1,150 people, planned
Started
10 Aug 2025
Expected to end
31 Aug 2027
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • Remote Ischemic Conditioning (RIC) treatment
  • Medical Management
Record updated
14 August 2025

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with a moderate ischemic stroke caused by a narrowed or blocked large artery, who can be randomized within 48 hours of the first symptoms.

Age
18 to 85 years old
Sex
Men and women can both join.
Disease stage
Ischemic stroke seen on MRI, within 48 hours of onset. NIHSS score 6-16, or 4-5 with disabling deficits. A large artery is 50%-99% narrowed or blocked. Before the stroke, mRS score of 0-1.
Earlier treatment
Thrombolysis or endovascular therapy for this stroke, done or planned, is not allowed.
Biomarker or test result
Narrowing of 50%-99% or blockage of a large artery, shown by MRA, CTA or DSA.

Main reasons for not taking part

  • Heart-related source of the stroke, such as atrial fibrillation or a recent heart attack
  • Uncommon causes of stroke, such as arterial dissection or Moyamoya disease
  • Dialysis, or severe kidney problems
  • Pregnancy
  • Any condition that rules out Remote Ischemic Conditioning, such as an arm fracture or arm vein thrombosis

The registry criteria, word for word

Show all 21 criteriaShow less

Who can take part

  • Male or female with age from 18 to 85 years old
  • Randomization must be within 48 hours after stroke symptom onset
  • Ischemic stroke confirmed by MRI diffusion-weighted imaging
  • NIHSS score 6-16, or 4-5 with disabling deficits at the time of randomization. The following typically should be considered disabling deficits: Complete hemianopsia (≥2 on NIHSS question 3) or severe aphasia (≥2 on NIHSS question 9), or visual or sensory extinction (≥1 on NIHSS question 11) or any weakness limiting sustained effort against gravity (≥2 on NIHSS question 6 or 7)
  • Proven large vessel 50%-99% stenosis or occlusion by MRA, CTA or DSA in cervical or intracranial carotid artery, M1 or M2 segments of the middle cerebral artery, A1 segment of anterior cerebral artery, P1 segment of posterior cerebral artery, vertebral artery, or basilar artery. For patients with single cerebral infarction, when MRA indicates >50% stenosis rather than occlusion, CTA or DSA should be performed to exclude the risk of MRA overestimating stenosis severity. Acute neurological deficit and cerebral infarction are compatible with ischemia in the vascular territory
  • Pre-stroke modified Rankin Scale score (mRS) of 0-1
  • Signed Informed Consent obtained

Who cannot take part

  • Thrombolysis or endovascular therapy performed or planned for index event
  • Suspected or confirmed cardioembolic source of stroke: i. The aetiology of cardiogenic embolism with high embolic potential, such as atrial fibrillation, atrial flutter, rheumatic mitral or aortic stenosis, artificial heart valve, left atrial myxoma, valve neoplasm, left ventricular wall thrombus, congestive heart failure, bacterial endocarditis, cardiomyopathy, myocardial infarction within previous 30 days; ii. Multiple cerebral infarctions in more than one vascular territory (e.g., bilateral MCA, or an MCA and a basilar artery) confirmed MRI diffusion-weighted imaging
  • Suspected or confirmed uncommon causes of cerebrovascular disorders: arterial dissection, Moyamoya disease, vasculitis disease, neurosyphilis, radiation induced vasculopathy, fibromuscular dysplasia, benign angiopathy of central nervous system, post-partum angiopathy, suspected vasospastic process, suspected recanalized embolus etc
  • Subclavian artery stenosis ≥ 50% or subclavian steal syndrome
  • Refractory hypertension (defined as persistent systolic blood pressure >185 mmHg or diastolic blood pressure >110 mmHg after drug treatment)
  • Respiratory failure, including type I and type II
  • Any contraindication for Remote Ischemic Conditioning: severe soft tissue injury, fracture, peripheral vascular disease, arteriovenous fistula, or venous thrombosis in the upper limbs
  • Severe comorbid condition with life expectancy < 6 months;
  • Patients with bleeding propensity: platelet count <50×10\^9/L; heparin was administered within 48 hours with APTT≥35s; on anticoagulant therapy with warfarin and International Normalized Ratio (INR) > 1.7
  • Undergoing hemodialysis or peritoneal dialysis, or known severe renal insufficiency with glomerular filtration rate <30 ml/min or serum creatinine >220 mmol/L (2.5mg/dl)
  • Evidence of intracranial tumor (except small meningioma), abscess, arteriovenous malformation
  • Current participation in any other investigational trial;
  • Pregnancy;
  • Patients not suitable for this clinical study considered by researchers

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 85 years old?

Where in China

  • The First Affiliated Hospital of Xi'an Jiaotong UniversityXi’an, ChinaContact: Suhang ShangTaking people

About the trial

What the trial wants to find out

Large Artery Atherosclerosis is one of the most prevalent causes of stroke worldwide and is associated with a high risk of disability and recurrent strokes. Remote Ischemic Conditioning (RIC) is a promising therapy, and it has been recommended for further investigation in patients with acute ischemic stroke resulting from large artery atherosclerosis. The primary objective of this study is to assess the efficacy of RIC in patients suffering from acute moderate ischemic stroke due to large artery atherosclerosis.

The 2 groups in the trial

  • Remote Ischemic Conditioning + Medical ManagementTreatment being tested

    Patients in this group will receive Remote Ischemic Conditioning plus best medical management.

    Treatment: Remote Ischemic Conditioning (RIC) treatment and Medical Management

  • Medical ManagementExisting treatment, for comparison

    Patients in this group will receive best medical management alone.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Remote Ischemic Conditioning for Acute Moderate Ischemic Stroke Due to Large Artery Atherosclerosis: A Multi-centered, Open-label, Blind Endpoint, Randomized Controlled Trial
Plain-language title
Remote Ischemic Conditioning Tested for Acute Moderate Stroke From Artery NarrowingGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Fit questions
Built from NCT06775782, who can take part
Record updated
14 August 2025