Skip to content

Clinical study of central combined with peripheral magnetic nerve stimulation on rehabilitation of motor function in patients with ischemic stroke

Clinical study of central combined with peripheral magnetic nerve stimulation on rehabilitation of motor function in patients with ischemic stroke

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047145
Enrollment
Unknown
Registered
2021-06-08
Start date
2021-06-09
Completion date
Unknown
Last updated
2022-01-24

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

Conditions

stroke

Interventions

Magnetic stimulation group:Magnetic stimulation
Magnetic stimulation group of two point:Magnetic stimulation
Fake Magnetic stimulation group:Fake Magnetic stimulation

Sponsors

Shanghai Minhang District Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with stroke by clinical evaluation and comprehensive imaging examination met the diagnostic criteria established by the National Cerebrovascular Academic Conference in 2014; 2. Fugl-Meyer motor function score was confirmed to be motor dysfunction, and >1 in the joint exercise assessment item; 3. Aged from 18 to 70 years, male or female; 4. No cognitive impairment or communication impairment, simple mental status test (MMSE) more than 27 points; 5. First onset, course of disease 2 days to 6 months.

Exclusion criteria

Exclusion criteria: 1. Patients with heart and lung diseases and other serious systemic diseases who cannot tolerate rehabilitation treatment; 2. Diagnosed with mental illness, major depression (suicidal tendencies) or epilepsy, with a family history of mental illness or epilepsy; 3. Diabetes, uremia and other serious systemic diseases; 4. Severe joint contracture; 5. Suffer from any cause of consciousness disorder; 6. According to the safety guidelines have transcranial direct current/magnetic stimulation (TMS/TDCS) and functional magnetic resonance (fMRI) examination of contraindications such as: there are metal foreign bodies in the body or other implants in the body of electronic devices; 7. Hearing or visual impairment may affect assessment and treatment; 8. The application of drugs to change the excitability of the cerebral cortex (antiepileptic drugs, sedative and hypnotic drugs, etc.).

Design outcomes

Primary

MeasureTime frame
pper limb Fugl-Meyer motor function score and changes;

Secondary

MeasureTime frame
Muscle strength score of affected limb;Modified Barthel Index;Hand function assessment;Electrophysiological examination of affected side nerve;Near-infrared functional imaging;

Countries

China

Contacts

Public ContactZhao Jing
dxu0927@163.com+86 13817103619

Outcome results

None listed

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