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A comparative study of the efficacy of cerebellar and cerebral motor cortex rTMS in the treatment of post

A comparative study of the efficacy of cerebellar and cerebral motor cortex rTMS in the treatment of post

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070532
Enrollment
Unknown
Registered
2023-04-14
Start date
2023-04-20
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Post-stroke combined swallowing disorder

Interventions

Experimental group:1. Stimulation frequency selection: repetitive transcranial magnetic stimulation (rTMS) at 10 Hz. 2. Stimulation site selection:Experimental group G1 selected the patient's bilatera
Control group:1. stimulation frequency selection: 10Hz repetitive transcranial magnetic stimulation (rTMS). 2. Stimulation site selection:The control group selected patients with bilateral cortical mo

Sponsors

The First Affiliated Hospital of Gannan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age = 18 years, regardless of gender; 2) first-onset stroke combined with dysphagia; 3) Swallowing disorder lasting from 2 weeks to 3 months; 4) Patients or their immediate family members voluntarily participated in this study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Suffering from serious diseases of the heart, liver, kidneys, etc., with unstable vital signs; 2) Patients who are taking antiepileptic, antidepressant and other sedative drugs; 3) Patients with tracheotomy or tracheal intubation; 4) with cranial defects or post-operative cranial repair 5) patients with intracranial metal built-ins or contraindications to transcranial magnetic stimulation therapy such as excessive intracranial pressure 6) Those who are participating in other clinical studies; 7) Patients with poor compliance and prone to missing visits; 8) Patients who, in the opinion of the investigator, are otherwise unsuitable for enrollment.

Design outcomes

Primary

MeasureTime frame
penetration-aspiration scale;Water Swallow Test;Clinical dysphagia score (CDS) ;

Secondary

MeasureTime frame
Modified Bathel Index;Functional Oral Intake Scale (FOIS);

Countries

China

Contacts

Public ContactLuo Yun

The First Affiliated Hospital of Gannan Medical University

735083566@qq.com+86 15754306145

Outcome results

None listed

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