Skip to content

To study the clinical observation and mechanism evaluation of electroacupuncture in the treatment of hemiplegic upper limb dyskinesia in cerebral infarction based on surface electromyography

To study the clinical observation and mechanism evaluation of electroacupuncture in the treatment of hemiplegic upper limb dyskinesia in cerebral infarction based on surface electromyography

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081781
Enrollment
Unknown
Registered
2024-03-12
Start date
2024-03-18
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

cerebral infarction

Interventions

Control Group:General acupuncture treatment

Sponsors

Beijing Rehabilitation Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) First onset, the lesion is located in one cerebral hemisphere, accompanied by one limb hemiplegia. (2) Those who meet the above diagnostic criteria of Chinese and Western medicine related to cerebral infarction, and have been confirmed by CT or MRI and other images, and the onset time is between 1 month and 6 months. (3) Patients with stage I soft paralysis of the affected upper limb. (4) Age 30-75 years old, male or female. (5) Patients with clear consciousness and stable vital signs. (6) There are no other acute diseases and serious complications. (7) Volunteer to participate in the research project and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with transient ischemic attack. (2) Patients with lesions involving bilateral cerebral hemispheres. (3) Patients who are still in acute coma, have serious encephalopathy, or complicated myocardial infarction, or have severe liver and kidney dysfunction, severe infection, serious diabetes, etc. (4) Patients with dementia, or those with severe sensory aphasia symptoms. (5) Dizzy needles, cannot cooperate with acupuncture; Or had started the systematic intervention of the experimental protocol for more than 1 week before enrollment. (6) Mental patients.

Design outcomes

Primary

MeasureTime frame
Upper limb FMA rating scale;

Secondary

MeasureTime frame
Modified Ashworth rating scale;Brunnstrom staging scale;Surface electromyography;

Countries

China

Contacts

Public ContactHongbo Zhao

Beijing Rehabilitation Hospital, Capital Medical University ,Capital Medical University School of Beijing Rehabilitation Medicine

172361285@qq.com+86 188 1046 5676

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026