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Comparison of cortical rTMS and cerebellar rTMS in the treatment of poststroke dysphagia

Comparison of cortical rTMS and cerebellar rTMS in the treatment of poststroke dysphagia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092432
Enrollment
Unknown
Registered
2024-11-15
Start date
2024-05-19
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

stroke

Interventions

control group:Repetitive transcranial magnetic stimulation of cortical region
Test group:Repetitive transcranial magnetic stimulation of cerebellum

Sponsors

Hanzhong Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) All the selected cases were in accordance with the "Diagnostic Key Points of Various Cerebrovascular Diseases" revised by the Fourth National Conference on Cerebrovascular Diseases of the Chinese Medical Association, and confirmed by craniocerebral CT or MRI, and diagnosed as ischemic or hemorrhagic unilateral stroke; ? 2 weeks = course =3 months and the condition was stable; ? Dysphagia lasting more than 2 weeks after stroke; (4) dysphagia disorder in the depression drinking test and VVST test; ? Assisted sitting posture for more than 30 minutes, speech and cognitive function is basically normal, can cooperate with various examinations and rehabilitation training. (6) Consent of patients and their families should be obtained before enrollment, and rTMS informed consent should be signed.

Exclusion criteria

Exclusion criteria: (1) Patients with swallowing dysfunction due to craniocerebral trauma or non-apoplexy neurological diseases such as Parkinson's disease; (2) Patients with dysphagia caused by lesions of swallowing organs or brain stem injury; (3) Local neck lesions, foreign bodies or related surgical treatment, such as thyroid disease, nasopharyngeal cancer, laryngeal cancer patients; (4) There are contraindications of rTMS, such as wearing a pacemaker or having metal in the brain; (5) Unstable arrhythmia; (6) Patients with a history of seizures; (7) Critically ill patients with fever, infection or vital organ failure; (8) Patients who cannot accept swallowing angiography (9) Those who cannot cooperate with assessment or treatment due to cognitive dysfunction or emotional reasons.

Design outcomes

Primary

MeasureTime frame
Standard Swallowing Function Evaluation Scale;Swallowing angiography rating scale;

Secondary

MeasureTime frame
water swallow test;Swallowing quality of life scale;

Countries

China

Contacts

Public ContactWang Yang

Hanzhong Central Hospital

516599293@qq.com+86 157 0926 0670

Outcome results

None listed

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