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Clinical study on paired associated magnetic stimulation therapy for post-stroke dysphagia

Clinical study on paired associated magnetic stimulation therapy for post-stroke dysphagia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110636
Enrollment
Unknown
Registered
2025-10-16
Start date
2025-11-30
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Post-stroke dysphagia

Interventions

TMS group:On the basis of conventional treatment, patients received rTMS (repetitive transcranial magnetic stimulation) therapy. The selection of TMS (transcranial magnetic stimulation) targets involv

Sponsors

Rehabilitation Medicine Department of Tangdu Hospital, Fourth Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The diagnosis of brainstem or cerebral hemisphere stroke is confirmed by cranial MRI; 2.Patients are assessed to have pharyngeal or oropharyngeal dysphagia through swallowing videofluoroscopy; 3.The onset of symptoms is within 3 months; 4.Cognitive function is good (MMSE > 17), and the patient has good cooperation ability; 5.Vital signs are stable, with no severe cardiac, hepatic, or renal failure; 6.Informed consent for examination and treatment has been obtained from the patient and their family members.

Exclusion criteria

Exclusion criteria: 1.Patients with severe depression, personality disorders, or other psychiatric conditions that prevent them from cooperating with treatment; 2.Patients with swallowing dysfunction caused by other systemic neurological diseases or malignant tumors of the head and neck; 3.Patients who had swallowing difficulties or coughing when drinking water prior to the onset of this illness; 4.Pregnant women; 5.Patients with contraindications to TMS, such as those with intracranial metal implants, brain tumors, or increased intracranial pressure.

Design outcomes

Primary

MeasureTime frame
Surface electromyography;

Secondary

MeasureTime frame
Rosenbek penetration aspiration scale;Excitatory test of swallowing motor pathway;

Countries

China

Contacts

Public ContactLiu Rui

Tangdu Hospital of the Fourth Military Medical University

tdliurui@fmmu.edu.cn+86 29 8477 7756

Outcome results

None listed

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