Arm cuff trick may shield brain during neck surgery
NCT ID NCT06033963
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a simple procedure called remote ischemic conditioning (RIC) in 100 people with narrowed neck arteries who were having surgery to clear the blockage. RIC involves briefly inflating a blood pressure cuff on both arms to temporarily stop blood flow, then releasing it, repeated several times. The goal was to see if this could reduce tiny brain injuries (seen on MRI) that sometimes happen during surgery. The trial is already completed, and results will show if this easy, low-cost technique is safe and worth studying further.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Remote ischemic conditioning (RIC) - a procedure using a blood pressure cuff to temporarily restrict blood flow to the arms
- What this could lead to
- If it works, RIC could become a simple, low-cost way to protect the brain during carotid artery surgery, reducing the risk of stroke or silent brain injury.
- What could go wrong
- This is a small pilot study (100 people) that is already completed, so results may not be definitive. The benefit may be small or not exist, and the procedure might not be practical for all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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100 people
The number who actually took part.
- Started
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Nov 2023
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age≥18 years, \<80 years, regardless of sex; 2. Symptomatic or asymptomatic carotid artery stenosis. In symptomatic patients the degree of stenosis should more than 50% (Based on North American Symptomatic Carotid Endarterectomy Trial Collaborators (NASCET) Criteria), in asymptomatic patients the degree of stenosis should more than 70% (Based on NASCET Criteria); 3. Baseline mRS 0-2; 4. Can cooperate with and complete brain magnetic resonance imaging (MRI) examination; 5. Signed and dated informed consent is obtained; Exclusion Criteria: 1. Evolving stroke; 2. Chronic complete occlusion of the carotid artery without obvious symptoms of cerebral ischemia; 3. Severe dementia; 4. The causes of cardiogenic embolism, such as rheumatic mitral or aortic valve stenosis, artificial heart valves, atrial fibrillation, atrial flutter, sick sinus syndrome, left atrial myxoma, left ventricular wall thrombosis or valve tumor, congestive heart failure, bacterial endocarditis, etc; 5. Uncontrolled hypertension (defined as systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 110 mmHg, despite medication taken at enrollment); 6. Severe hepatic and renal dysfunction (defined as aspartate aminotransferase (AST) or alanine aminotransferase (ALT) ≥3 times higher than the upper limit of the normal range, creatinine \>265umol/l (3mg/dl)); 7. The patients who have the contraindication of remote ischemic conditioning treatment, such as severe soft tissue injury, fracture or vascular injury in the upper limb. Acute or subacute venous thrombosis, arterial occlusive disease, subclavian steal syndrome, etc; 8. Pregnant or lactating women; 9. He/She is participating in other clinical research or has participated in other clinical research or has participated in this study within 3 months prior to admission; 10. Other conditions that the researchers think are not suitable for the group.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The First Hospital of Jilin University
Changchun, Jilin, 130000, China
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Other studies related to the condition(s) this trial covers.
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