Clinical Trial on the Safety and Efficacy of Optimized Transcranial Direct Current Stimulation for the Swallowing Function in Patients With Post-Stroke Dysphagia

NARecruitingINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

April 22, 2024

Primary Completion Date

July 31, 2025

Study Completion Date

December 31, 2025

Conditions
Deglutition Disorders
Interventions
DEVICE

Optimized transcranial Direct Current Stimulation

transcranial Direct Current Stimulation 2mA for 30 min; The anode electrode will be located over the contralesional representation of the motor cortex swallowing area, while the cathode electrode will be positioned on the ipsilesional side

DEVICE

Sham transcranial Direct Current Stimulation

transcranial Direct Current sham Stimulation for 30 min; The anode electrode will be located over the contralesional representation of the motor cortex swallowing area, while the cathode electrode will be positioned on the ipsilesional side

Trial Locations (1)

14647

RECRUITING

The Catholic University of Korea, Bucheon St. Mary's Hospital, Bucheon-si

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Bucheon St. Mary's Hospital

OTHER

collaborator

Saint Vincent's Hospital, Korea

OTHER

collaborator

National Traffic Injury Rehabilitation Hospital

UNKNOWN

collaborator

Pusan National University Yangsan Hospital

OTHER

lead

NEUROPHET

INDUSTRY

NCT06305949 - Clinical Trial on the Safety and Efficacy of Optimized Transcranial Direct Current Stimulation for the Swallowing Function in Patients With Post-Stroke Dysphagia | Biotech Hunter | Biotech Hunter