Effect of Remote Ischemic Postcondioning on Glymphatic System in Acute Stroke
NCT ID: NCT05305625
Last Updated: 2022-03-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2022-05-01
2023-05-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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standard therapy
Patients will be treated with Guideline standard
standard therapy
received standardized treatment
remote ischemic postcondioning and standard therapy
Patients will be treated with remote ischemic postcondioning and Guideline standard , remote ischemic postcondioning twice a day for a total of 3 days.
remote ischemic postcondioning
remote ischemic postcondioning twice daily, for three consecutive days，the upper arm of the lighter paralyzed side was pressurized to 200mmHg, pressurized 5min and relaxed for 5 minutes for 4 cycles as a complete remote ischemic postcondioning
standard therapy
received standardized treatment
Interventions
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remote ischemic postcondioning
remote ischemic postcondioning twice daily, for three consecutive days，the upper arm of the lighter paralyzed side was pressurized to 200mmHg, pressurized 5min and relaxed for 5 minutes for 4 cycles as a complete remote ischemic postcondioning
standard therapy
received standardized treatment
Eligibility Criteria
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Inclusion Criteria
* The NIHSS score was ≤ 25 and NIHSS \> 5，Glasgow coma score ≥ 8;
* The patients were diagnosed as anterior circulation cerebral infarction and could start remote ischemic postcondioning within 24 hours after onset
* Normal to random time within 24 hours
* Written informed consent signed by patients or their families
Exclusion Criteria
* modified Rankin scale (mRS) score ≥ 2 before this attack;
* other intracranial lesions, such as cerebral hemorrhage, cerebral venous disease, severe subclavian artery stenosis and other diseases involving the brain;
* Arterial blood pressure ≤ 90/60mmHg or ≥ 180/100mmHg after treatment.
18 Years
80 Years
ALL
No
Sponsors
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The Affiliated Hospital of Xuzhou Medical University
OTHER
Responsible Party
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Central Contacts
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Other Identifiers
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XYFY2022-KL026
Identifier Type: -
Identifier Source: org_study_id