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Clinical Trials/NCT06033963
NCT06033963
Completed
Not Applicable

Safety and Efficacy of Remote Ischemic Conditioning in Patients With Carotid Artery Stenosis Undergoing Carotid EndArterectomy: A Pilot, Randomized Controlled Trial

Yi Yang1 site in 1 country100 target enrollmentNovember 20, 2023

Overview

Phase
Not Applicable
Intervention
Remote ischemic conditioning
Conditions
Carotid Artery Stenosis
Sponsor
Yi Yang
Enrollment
100
Locations
1
Primary Endpoint
Proportion of patients who got ≥1 new Diffusion Weighted Imaging (DWI)-positive lesions on post-treatment magnetic resonance imaging (MRI) Scans.
Status
Completed
Last Updated
2 months ago

Overview

Brief Summary

The purpose of this study is to explore the safety and efficacy of remote ischemic conditioning in patients with carotid artery stenosis undergoing carotid endarterectomy.

Detailed Description

In this study, 100 patients with carotid artery stenosis undergoing carotid endarterectomy are included in our center in China according to the principle of random, and parallel control. The experimental group receive basic treatment and remote ischemic conditioning for 200mmHg, 2 times per day for 6 consecutive days. The control group receive basic treatment and remote ischemic conditioning control for 60mmHg, 2 times per day for 6 consecutive days. Two groups will be followed up for 1 year to evaluate the safety and efficacy of remote ischemic conditioning in patients with carotid artery stenosis undergoing carotid endarterectomy.

Registry
clinicaltrials.gov
Start Date
November 20, 2023
End Date
December 11, 2025
Last Updated
2 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Yi Yang
Responsible Party
Sponsor Investigator
Principal Investigator

Yi Yang

Associated Dean of First Hospital of Jilin University

The First Hospital of Jilin University

Eligibility Criteria

Inclusion Criteria

  • Age≥18 years, \<80 years, regardless of sex;
  • 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);
  • Baseline mRS 0-2;
  • Can cooperate with and complete brain magnetic resonance imaging (MRI) examination;
  • Signed and dated informed consent is obtained;

Exclusion Criteria

  • Evolving stroke;
  • Chronic complete occlusion of the carotid artery without obvious symptoms of cerebral ischemia;
  • Severe dementia;
  • 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;
  • Uncontrolled hypertension (defined as systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 110 mmHg, despite medication taken at enrollment);
  • 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));
  • 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;
  • Pregnant or lactating women;
  • 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;
  • Other conditions that the researchers think are not suitable for the group.

Arms & Interventions

RIC+CEA+Standard medical treatment

Remote ischemic conditioning (RIC) is induced by 5 cycles of 5 min of bilateral upper limbs ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflation of a blood pressure cuff to 200 mmHg. RIC will be conducted twice daily for 6 consecutive days after enrollment. Additionally, the patients will be treated with carotid endarterectomy (CEA) and standard medical treatment according to the Chinese guideline for the secondary prevention of ischemic stroke and transient ischemic attack 2022.

Intervention: Remote ischemic conditioning

Sham RIC+CEA+Standard medical treatment

Remote ischemic conditioning (RIC) is induced by 5 cycles of 5 min of bilateral upper limbs ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflation of a blood pressure cuff to 60 mmHg. RIC will be conducted twice daily for 6 consecutive days after enrollment. Additionally, the patients will be treated with carotid endarterectomy (CEA) and standard medical treatment according to the Chinese guideline for the secondary prevention of ischemic stroke and transient ischemic attack 2022.

Intervention: Sham remote ischemic conditioning

Outcomes

Primary Outcomes

Proportion of patients who got ≥1 new Diffusion Weighted Imaging (DWI)-positive lesions on post-treatment magnetic resonance imaging (MRI) Scans.

Time Frame: 6 days

Patients underwent magnetic resonance imaging (including DWI)at baseline and 6 days after randomization.

Secondary Outcomes

  • The number of new Diffusion Weighted Imaging (DWI)-positive lesions on post-treatment magnetic resonance imaging (MRI) Scans.(6 days)
  • The volume of new Diffusion Weighted Imaging (DWI)-positive lesions on post-treatment magnetic resonance imaging (MRI) Scans.(6 days)
  • Proportion of patients with any side effects of Remote ischemic conditioning (RIC) treatment.(6 days)
  • Number of patients with cerebrovascular events, cardiovascular events or death.(1 year)

Study Sites (1)

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