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A Study on the Efficacy of Transcutaneous Vagus Nerve Stimulation in Improving Swallowing Disorders in Post-Stroke Patients

A Study on the Efficacy of Transcutaneous Vagus Nerve Stimulation in Improving Swallowing Disorders in Post-Stroke Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108870
Enrollment
Unknown
Registered
2025-09-08
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Dysphagia

Interventions

Experimental group:The stimulation parameters use 25Hz bidirectional pulses with a pulse width of 250µs, and the treatment time is 20 minutes. The range of stimulation intensity is 0-5mA. Auricular st
Control group:The stimulation parameters use 25Hz bidirectional pulses with a pulse width of 250µs, and the treatment time is 20 minutes. The range of stimulation intensity is 0-5mA. Sham stimulation

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with first onset stroke diagnosed by computed tomography (CT) or magnetic resonance imaging (MRI) aged 30 to 80 years, with onset time of 2 weeks to 12 months; 2. Water drinking test score >= 3 points; 3. No history of neurological diseases or swallowing disorders prior to the current onset; 4. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe heart, lung, and liver dysfunction; 2. Unconsciousness, severe cognitive impairment, unable to cooperate with treatment; 3. Diseases of the esophagus and throat structures themselves; 4. Low heart rate (60 beats per minute) or previous vagus nerve surgical intervention.

Design outcomes

Primary

MeasureTime frame
Digital image analysis of videofluoroscopic swallowing study (VFSS);

Countries

China

Contacts

Public ContactFan Yu

Shanghai General Hospital

dr_yufan@163.com+86 177 0175 2339

Outcome results

None listed

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