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Clinical Trials/NCT02323425
NCT02323425
Unknown
Not Applicable

Effects of Upper Limb Ischemic Postconditioning on Collateral Circulation in Young Symptomatic Intracranial Atherosclerosis

Health Science Center of Xi'an Jiaotong University1 site in 1 country100 target enrollmentMarch 2015
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Health Science Center of Xi'an Jiaotong University
Enrollment
100
Locations
1
Primary Endpoint
Mean Change of Collateral Circulation from Baseline and at 6 months
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the protective effects of upper limb ischemic postconditioning on collateral circulationin young symptomatic intracranial atherosclerosis and the baseline characteristics of trial participants, as an open, randomized controlled, prospective controlled trial.

Detailed Description

Stroke is a common cardia-cerebrovascular disease with high morbidity, disability and mortality rate. And more and more young patients account for the increasing morbidity. Among them, Symptomatic intracranial atherosclerotic stenosis(sICAS)is a major cause, especially in Asians. Currently, traditional therapeutic methods present reluctant achievements on reducing stroke recurrence and pose threat on patients'health because of invasive operation and severe side effects. Therefore, other treatment methods are called for urgently. Remote ischemic post-conditioning refers to local or distal ischemia treatment after the occurrence of cerebral ischemia. Prior research has shown that repeatedly ischemic reperfusion have protective effect on lowering the occurrence rate of ischemic events of patients with carotid stenosis. However, in-depth research on cerebral protection and correlation with collateral circulation has not been proven in an open, definitive clinical trial. Thus, the EPIC-sICAS trial will provide important information on the protective effects of upper limb ischemic post-conditioning on collateral circulation after cerebral Infarction. Hopefully to present us a very meaningful way to improve the patient's quality of life.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
March 2018
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Health Science Center of Xi'an Jiaotong University
Responsible Party
Principal Investigator
Principal Investigator

Meng Wei

Director, Clinical Research

Health Science Center of Xi'an Jiaotong University

Eligibility Criteria

Inclusion Criteria

  • Age between 18 to 45 Years old;
  • Symptomatic intracranial atherosclerotic stenosis (sICAS): cranial CTA/MRA/TCD/DSA confirm the diagnosis, patients got ischemic stroke or transient ischemic attack in the brain region supplied by the stenosis artery;
  • National Institutes of Health Stroke Scale(NIHSS) score 0-15
  • Written informed consent was signed.

Exclusion Criteria

  • Cerebral hemorrhage and other parts of the active bleeding disease;
  • Severe aphasia, unable to express himself;
  • A history of brain tumor, brain trauma, cerebral embolism or other brain lesions;
  • Severe lesions of severe cardiac, liver or kidney disease, malignancy or other systemic organ dysfunction;
  • Blood Pressure\< 90 mmHg/60 mmHg or \>200 mmHg/110 mmHg after treatment;
  • Dementia and mental illness;
  • Using angiotensin-converting enzyme inhibitors;
  • A history of major surgery or trauma 4 weeks prior to admission;
  • Without informed consent.
  • Elimination Criteria:

Outcomes

Primary Outcomes

Mean Change of Collateral Circulation from Baseline and at 6 months

Time Frame: Baseline and at 6 months

Collateral circulation measured in iconography test: Magnetic Resonance Angiography (MRA)、 Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI)、Arterial spin-labeled (ASL) perfusion magnetic resonance、Transcranial Cerebral Doppler (TCD)、single photon emission computed tomography(SPECT) Baseline was defined as the onset of stroke within 48h. A higher score represents better collateral circulation status functioning.

Secondary Outcomes

  • Mean Change of Symptomatic Recovery(Baseline and at 14 days, 1 month, 6 months, and 1 year)
  • Mean Change of serum vascular endothelial growth factor (VEGF) and basic Fibroblast Growth Factor (bFGF) from Baseline and at 10 days.(Baseline and at 10 days)

Study Sites (1)

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