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Effects of bilateral high-frequency repetitive transcranial magnetic stimulation on swallowing function in stroke patients

Effects of bilateral high-frequency repetitive transcranial magnetic stimulation on swallowing function in stroke patients

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061871
Enrollment
Unknown
Registered
2022-07-05
Start date
2022-06-20
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Dysphagia after stroke

Interventions

Control group:Routine rehabilitation training
Experimental group:Bilateral 10 Hz transcranial magnetic stimulation

Sponsors

The First Affiliated Hospital of Bengbu Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The patients met the diagnostic criteria formulated by the 4th National Conference on Cerebrovascular Diseases, and were confirmed by CT or MRI examination, and were patients with subcortical stroke; 2. Aged 35-80 years; 3. Course of disease: 2 weeks to 6 months; 4. The drinking water test screening level 2 and below; 5. Stable vital signs, clear consciousness, able to execute treatment instructions and cooperate in completing treatment and assessment; 6. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Previous intracranial diseases such as brain trauma and encephalitis; 2. Those who cannot complete the index evaluation, such as severe aphasia, severe cognitive impairment, audio-visual impairment, illiteracy, etc.; 3. Tthe existence of organic swallowing dysfunction; 4. Tomplicated with serious primary diseases of cardiovascular, liver, kidney and hematopoietic systems; 5. Other clinical experimenters who are participating in influencing the results of this study; 6. having a pacemaker or cochlear implant, implanted device (e.g. deep brain stimulator, ventriculoperitoneal shunt) or metal in the brain (e.g., aneurysm clip); 7. Patients with epilepsy or their families; 8. rTMS contraindications; 9. Quit the study due to uncontrollable factors.

Design outcomes

Primary

MeasureTime frame
SEMG assessment of deglutition-related muscle groups;Wata drinking water experiment;

Countries

China

Contacts

Public ContactWangMin

The First Affiliated Hospital of Bengbu Medical College

1239196714@qq.com+86 15178368168

Outcome results

None listed

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