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Effect of Remote Ischemic Postcondioning on Glymphatic System in Acute Stroke

X

Xuzhou Medical University

Status

Unknown

Conditions

Stroke

Treatments

Procedure: remote ischemic postcondioning
Drug: standard therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05305625
XYFY2022-KL026

Details and patient eligibility

About

Investigators aimed to investigate the changes of glymphatic function after remote ischemic postcondioning treatment in acute ischemic stroke .

Enrollment

60 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patient was 18-80 years old;
  • 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

  • patients receiving thrombolysis or endovascular therapy;
  • 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

standard therapy
Experimental group
Description:
Patients will be treated with Guideline standard
Treatment:
Drug: standard therapy
remote ischemic postcondioning and standard therapy
Experimental group
Description:
Patients will be treated with remote ischemic postcondioning and Guideline standard , remote ischemic postcondioning twice a day for a total of 3 days.
Treatment:
Procedure: remote ischemic postcondioning
Drug: standard therapy

Trial contacts and locations

0

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Central trial contact

Yu Lu, MD

Data sourced from clinicaltrials.gov

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