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Randomized controlled study of acupuncture combined with rehabilitation training on limb function and emotion of patients with spastic hemiplegia after ischemic stroke

Phase 1
Recruiting
Conditions
Spastic Hemiplegia after ischemic stroke
Registration Number
ITMCTR2000004195
Lead Sponsor
Dongfang Hospital of Beijing University of traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1. Patients with ischemic stroke diagnosed by traditional Chinese and Western medicine and confirmed by head CT or MRI;
2. Patients with clinical neurological deficit score (NFDS) between 0 and 30;
3. For patients with hemiplegia, monoplegia or hypermyotonia, the modified Ashworth rating was 1-3;
4. Patients who have been ill for 72 hours to 6 months;
5. Patients aged 35 to 85;
6. The first stroke was the main one, and if it was a recovery, there was no limb movement dysfunction in the past;
7. Patients with informed consent.

Exclusion Criteria

1. Patients with transient ischemic attack (TIA), reversible ischemic neurological deficit (rind) and complete recovery ischemic attack;
2. Patients with cerebral hemorrhage and subarachnoid hemorrhage;
3. Patients with severe cerebral edema or coma due to massive cerebral infarction, etc;
4. Patients with stroke caused by brain tumor, brain trauma and blood disease confirmed by examination;
5. Patients with cerebral embolism caused by rheumatic heart disease, coronary heart disease and other heart diseases complicated with atrial fibrillation;
6. Patients with severe infection or severe diseases such as liver, kidney, hematopoietic system, endocrine system, and osteoarthritis with severe osteoporosis or affecting functional recovery;
7. Patients with quadriplegia;
8. Patients with severe mental symptoms, severe cognitive impairment and dementia;
9. Patients currently participating in other research treatments.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
CSI;MAS;DTI;ADL;FMA;
Secondary Outcome Measures
NameTimeMethod
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