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Clinical Trials/ITMCTR2100004539
ITMCTR2100004539
Recruiting
Phase 1

sing resting-state functional magnetic resonance imaging to investigate a central mechanism of contralateral acupuncture at Hand-Yangming in patients with cerebral ischemic stroke

Hospital of Chengdu University of Traditional Chinese Medicine0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Cerebral ischemia stroke
Sponsor
Hospital of Chengdu University of Traditional Chinese Medicine
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
All

Investigators

Sponsor
Hospital of Chengdu University of Traditional Chinese Medicine

Eligibility Criteria

Inclusion Criteria

  • (1\) Corresponding to the diagnostic standards of cerebral ischemic stroke(Referring to the 2019 version cerebral vascular disease diagnostic criteria) and diagnosed with CIS and confirmed by CT or MRI, occurred \>\= 2 weeks and \<\= 6 months previously, stable vital sign and consciousness without disorders of language;
  • (2\) According to the OCSP clinical classification standard, it is partial anterior circulation infarction (PACI), and the lesion is mainly on the right basal ganglia and/or corona radiata;
  • (3\) The initial onset, hemiplegia existed in one limb, NIHSS score \>\= 3 and \< 10 or(and) the upper limbs function score of Brunnstrom stages recovery at the stage 1\-5;
  • (4\) Aged between 35 and 75 years;
  • (5\) Informed consent signed by the patient or by the patient's relative;
  • (6\) Patients who have better compliance and can complete the research.

Exclusion Criteria

  • (1\) Course of disease \> 6 months, or advanced acute stroke, or unstable vital sign;
  • (2\) Persons with Wernicke's aphasia, severe cognitive impairment, mental illnesses or post\-stroke depression.
  • (3\) Patients with severe heart, lung, liver, and kidney diseases;
  • (4\) Patients have pacemakers and metal implants in the body and underwent bypass operation or can't undergo MRI;
  • (5\) Persons with skin disease and coagulation dysfunction;
  • (6\) Pregnant women or women in puerperium;
  • (7\) Patients who can't cooperate with treatment, observation and examination.
  • (8\) Participants in other clinical tests at the same time.

Outcomes

Primary Outcomes

Not specified

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