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Multimodal Magnetic Resonance Imaging Study for the Mechanism of Bilateral Brain Remodeling and Acupuncture Promoting Hemiplegia Rehabilitation

Multimodal Magnetic Resonance Imaging Study for the Mechanism of Bilateral Brain Remodeling and Acupuncture Promoting Hemiplegia Rehabilitation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022220
Enrollment
Unknown
Registered
2019-03-30
Start date
2019-04-01
Completion date
Unknown
Last updated
2020-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hemiplegia after cerebral infarction

Interventions

Paralysis study group (the first scan):true acupuncture stimulation
Paralysis study group (the first scan):sham acupuncture stimulation
Paralysis study group (the second scan):Contrary to the first scan
Healthy control group(the first scan):true acupuncture stimulation
Healthy control group(the first scan):sham acupuncture stimulation
Healthy control group(the second scan):Contrary to the first scan

Sponsors

Dongzhimen Hospital, Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Hemiplegia patients test group Diagnostic criteria: Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2014. (1) Patients with cerebral infarction whose course of disease is 1.5 months conform to the diagnostic criteria of cerebral infarction; (2) Right-handed; (3) Between 40 and 75 years of age, both men and women are eligible; (4) In patients with left hemiplegia, the infarct was located in the right basal ganglia and/or the radiation coronal region; (5) The patient has unconscious disorder and the condition is relatively stable; (6) No psychotropic drugs have been taken in the past month; (7) Here is no metal in the body and no contraindication of nuclear magnetic resonance examination; (8) The patient himself or his immediate family members sign the informed consent; 2. Healthy subjects group: (1) Right-handed; (2) Between 40 and 75 years of age, both men and women are eligible; (3) Those who have been proved to be in the range of physical health by physical examination have no organic or significant functional diseases; (4) No family genetic history of mental and nervous system; (5) No research similar to this experiment has been conducted. (6) There were no physical abnormalities (such as cold, headache, cough, etc.) during the experimental period. (7) No excitatory drugs have been taken in the past two months. (8) There are no metal implants in vivo and no contraindications for functional magnetic resonance imaging. (9) Subjects signed the informed consent and volunteered to participate in the experiment.

Exclusion criteria

Exclusion criteria: 1.Hemiplegia patients test group (1)combining with psychiatric disorders or any other serious primary diseases; (2)being pregnant, lactating or menstrual; (3)severe skull anatomical asymmetry or definite lesions being found by MRI scans; (4)taking part in similar neuroimaging test within 1 month. 2.Healthy subjects group: (1)being menstrual, pregnant or lactating; (2)severe skull anatomical asymmetry or definite lesions being found by MRI scans.

Design outcomes

Primary

MeasureTime frame
functional connectivity(FC);

Secondary

MeasureTime frame
Voxel-mirrored homotopic connectivity (VMHC);Fractional anisotropy (FA);Voxel-Based Morphometry(VBM);Fugl-Meyer Assessment;hs-CRP;

Countries

China

Contacts

Public ContactYihuai Zou

Dongzhimen Hospital, Beijing University of Chinese Medicine

zouyihuai2004@163.com+86 010-84013130

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026