Remote Ischemic Conditioning for Acute Moderate Ischemic Stroke (RICAMIS)
Primary Purpose
Stroke
Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Remote Ischemic Conditioning treatment
Guideline-based therapy
Sponsored by
About this trial
This is an interventional treatment trial for Stroke
Eligibility Criteria
Inclusion Criteria:
- Patient age ≥18 years;
- From onset to treatment ≤ 48 hours;
- Ischemic stroke confirmed by head CT or MRI;
- 6≤NIHSS score ≤ 16;
- Premorbid mRS ≤ 1;
- Signed informed consent.
Exclusion Criteria:
- Serious neurological deficits before onset ( mRS ≥ 2);
- The aetiology of cardiogenic embolism, such as rheumatic mitral or aortic stenosis, artificial heart valve, atrial fibrillation, atrial flutter, sick sinus syndrome, left atrial myxoma, left ventricular wall thrombus or valve neoplasm, congestive heart failure, bacterial endocarditis, etc;
- Uncontrolled severe hypertension (Systolic pressure ≥180 mmHg or diastolic pressure ≥110 mmHg after drug treatment);
- Subclavian artery stenosis ≥ 50% or subclavian steal syndrome;
- Intracranial tumor, arteriovenous malformation or aneurysm;
- Severe abnormalities in coagulation;
- Any contraindication for remote ischemic adaptation: the upper limb has serious soft tissue injury, fracture or vascular injury, distal upper limb perivascular lesions, etc.;
- Comorbidity with any serious diseases and life expectancy is less than half a year;
- Participating in other clinical trials within 3 months;
- Patients not suitable for this clinical studies considered by researcher;
Sites / Locations
- General Hospital of ShenYang Military Region
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Guideline-based therapy+RIC
Guideline-based therapy
Arm Description
RIC is given twice a day with 200mmHg pressure.
Outcomes
Primary Outcome Measures
Proportion of mRS (0-1)
Secondary Outcome Measures
Proportion of mRS (0-2)
Incidence of early neurological deterioration
more than 4 NIHSS score increase compared with baseline
Incidence of stroke associated pneumonia
occurrence of stroke or other vascular events
proportion of death of any cause
Full Information
NCT ID
NCT03740971
First Posted
November 12, 2018
Last Updated
May 4, 2021
Sponsor
General Hospital of Shenyang Military Region
1. Study Identification
Unique Protocol Identification Number
NCT03740971
Brief Title
Remote Ischemic Conditioning for Acute Moderate Ischemic Stroke
Acronym
RICAMIS
Official Title
Remote Ischemic Conditioning for Acute Moderate Ischemic Stroke (RICAMIS): a Prospective, Random, Open Label, Blinded End Point, Multi-center Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
December 26, 2018 (Actual)
Primary Completion Date
April 19, 2021 (Actual)
Study Completion Date
April 19, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
General Hospital of Shenyang Military Region
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The current treatment based on evidence-based medicine for acute ischemic stroke mainly includes reperfusion (intravenous thrombolysis, mechanical thrombolysis), anti-platelet and stroke units. About 1/3 patients can obtain good prognosis through intravenous thrombolysis. Good prognosis can be gotten from about 50 percent of patients with big artery disease by mechanical embolization. However, only a small proportion of the population can be treated with restoration perfusion in the time window. The main purpose of antiplatelet therapy is to prevent the recurrence and progression of stroke, and stroke unit is a kind of management mode. How to improve the neurological function of patients has been a hot and difficult problem in clinical practice.
A large number of basic and clinical studies have proved that remote ischemic conditioning (RIC) has protective effect on ischemic stroke. Hahn et al showed that RIC could play a neuroprotective role in cerebral ischemia-reperfusion injury in MCAO model. Other studies have also confirmed that preconditioning RIC has a neuroprotective effect on cerebral ischemia in animal models. One open label study by Hougaard et al shows that RIC can improve the NIHSS score in acute ischemic stroke patients. One recent study found that 300 consecutive days RIC therapy for the patients with symptomatic intracranial atherosclerotic stenosis significantly reduced the recurrence rate of stroke, improved the mRS score and recovered the blood flow in the lesion site. Furthermore, several studies have also shown that RIC can not only improve the neurological function of patients with cerebral infarction after intravenous thrombolysis and mechanical thrombolysis, but also protect the secondary brain injury after carotid stenting. These results suggest that RIC has a neuroprotective effect on ischemic stroke and deserves further study.
Based on the above discussion, this study aims to explore the efficacy and safety of RIC in the treatment of acute moderate ischemic stroke.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1800 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Guideline-based therapy+RIC
Arm Type
Experimental
Arm Description
RIC is given twice a day with 200mmHg pressure.
Arm Title
Guideline-based therapy
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
Remote Ischemic Conditioning treatment
Intervention Description
Remote Ischemic Conditioning is given twice a day with 200mmHg pressure.
Intervention Type
Drug
Intervention Name(s)
Guideline-based therapy
Intervention Description
Guideline-based therapy
Primary Outcome Measure Information:
Title
Proportion of mRS (0-1)
Time Frame
90±7 days
Secondary Outcome Measure Information:
Title
Proportion of mRS (0-2)
Time Frame
90±7 days
Title
Incidence of early neurological deterioration
Description
more than 4 NIHSS score increase compared with baseline
Time Frame
7 days
Title
Incidence of stroke associated pneumonia
Time Frame
12±2 days
Title
occurrence of stroke or other vascular events
Time Frame
90±7 days
Title
proportion of death of any cause
Time Frame
90±7 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient age ≥18 years;
From onset to treatment ≤ 48 hours;
Ischemic stroke confirmed by head CT or MRI;
6≤NIHSS score ≤ 16;
Premorbid mRS ≤ 1;
Signed informed consent.
Exclusion Criteria:
Serious neurological deficits before onset ( mRS ≥ 2);
The aetiology of cardiogenic embolism, such as rheumatic mitral or aortic stenosis, artificial heart valve, atrial fibrillation, atrial flutter, sick sinus syndrome, left atrial myxoma, left ventricular wall thrombus or valve neoplasm, congestive heart failure, bacterial endocarditis, etc;
Uncontrolled severe hypertension (Systolic pressure ≥180 mmHg or diastolic pressure ≥110 mmHg after drug treatment);
Subclavian artery stenosis ≥ 50% or subclavian steal syndrome;
Intracranial tumor, arteriovenous malformation or aneurysm;
Severe abnormalities in coagulation;
Any contraindication for remote ischemic adaptation: the upper limb has serious soft tissue injury, fracture or vascular injury, distal upper limb perivascular lesions, etc.;
Comorbidity with any serious diseases and life expectancy is less than half a year;
Participating in other clinical trials within 3 months;
Patients not suitable for this clinical studies considered by researcher;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huisheng Chen, Doctor
Organizational Affiliation
Neurology Department
Official's Role
Study Chair
Facility Information:
Facility Name
General Hospital of ShenYang Military Region
City
ShenYang
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
35972485
Citation
Chen HS, Cui Y, Li XQ, Wang XH, Ma YT, Zhao Y, Han J, Deng CQ, Hong M, Bao Y, Zhao LH, Yan TG, Zou RL, Wang H, Li Z, Wan LS, Zhang L, Wang LQ, Guo LY, Li MN, Wang DQ, Zhang Q, Chang DW, Zhang HL, Sun J, Meng C, Zhang ZH, Shen LY, Ma L, Wang GC, Li RH, Zhang L, Bi C, Wang LY, Wang DL; RICAMIS Investigators. Effect of Remote Ischemic Conditioning vs Usual Care on Neurologic Function in Patients With Acute Moderate Ischemic Stroke: The RICAMIS Randomized Clinical Trial. JAMA. 2022 Aug 16;328(7):627-636. doi: 10.1001/jama.2022.13123.
Results Reference
derived
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Remote Ischemic Conditioning for Acute Moderate Ischemic Stroke
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