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Clinical study for repeated transcranial magnetic stimulation (rTMS) at different positions in the treatment of dysphagia in stroke patients

Clinical study on the treatment of dysphagia in stroke patients with different parts of rTMS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032255
Enrollment
Unknown
Registered
2020-04-24
Start date
2020-04-25
Completion date
Unknown
Last updated
2020-04-27

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

Conditions

Stroke

Interventions

A:RTMS stimulates unaffected cortical areas of the suprahyoid muscles
B:RTMS stimulates affected cortical areas of the suprahyoid muscles
C:RTMS stimulates Cerebellar cortex

Sponsors

Yuebei People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients willing to sign informed consent; 2. Patients between 18 and 85 years old; 3. MRI confirmed the patients with the first stroke; 4. Patients with dysphagia found in clinical and instrument examination, less than 3 months; 5. Patients with stable basic disease process; 6. Patients with severe feeding dependent dysphagia who were confirmed to have dysphagia by standard swallowing assessment (SSA) or feas; 7. Patients diagnosed with dysphagia due to acute ischemic stroke are eligible for inclusion in the study within 24 hours of stroke onset. As long as there is no hemorrhagic transformation or obvious brain edema, there is no limit to the size and location of the infarction.

Exclusion criteria

Exclusion criteria: 1. Patients with cognitive impairment or mental depression; 2. Patients with neurodegenerative diseases; 3. Patients with unstable cardiopulmonary status; 4. Patients with tumor, extensive surgery or head and neck radiotherapy; 5. Patients with pacemaker or history of epilepsy or epilepsy; 6. Patients who had swallowing therapy before participating in this study; 7. Patients who need skull surgery before or at present; 8. Patients with any form of metal implants and tracheal intubation

Design outcomes

Primary

MeasureTime frame
FEDSS;

Secondary

MeasureTime frame
Rosenbek PAS;SSA;GUSS;DD;

Countries

China

Contacts

Public ContactHuiyu Liu

Yuebei People's Hospital

1045273455@qq.com+86 13922599818

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026