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A Comparative Study on Efficacy of Precise Navigation TMS Based on Real-World Data versus Conventional Localization TMS in Treating Post-Stroke Dysphagia

A Comparative Study on Efficacy of Precise Navigation TMS Based on Real-World Data versus Conventional Localization TMS in Treating Post-Stroke Dysphagia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126270
Enrollment
Unknown
Registered
2026-06-05
Start date
2026-06-05
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Post-stroke Dysphagia

Interventions

Navigated TMS Group:None
Conventional Localization TMS Group:None

Sponsors

Beijing Zhongguancun Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years old, regardless of gender. 2. Clinically diagnosed stroke (ischemic or hemorrhagic), confirmed by CT or MRI. 3. Suffering from post-stroke dysphagia verified via C-MASA scale, Kubota water swallow test and other assessments. 4. Receiving the first prescription of transcranial magnetic stimulation (TMS) issued by physicians from the Department of Rehabilitation of our hospital. 5. Capable of cooperating with assessments, follow-up visits and MRI examinations; no contraindications to MRI. 6. Signed written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Presence of absolute contraindications to TMS or MRI, including intracranial metallic implants, cardiac pacemakers, active epilepsy, claustrophobia, etc. 2. Complicated with severe progressive or terminal diseases with an expected survival of less than 6 months. 3. Concurrent participation in other interventional clinical trials that may interfere with swallowing function assessments. 4. Subjects unable to complete assessments and imaging examinations as required.

Design outcomes

Primary

MeasureTime frame
Chinese version of Mann Assessment of Swallowing Ability (C-MASA);

Secondary

MeasureTime frame
Chinese version of Mann Assessment of Swallowing Ability (C-MASA) at each follow-up time point;Functional Oral Intake Scale (FOIS) score;Swallowing Quality of Life (SWAL-QOL) score;Incidence of Adverse Events;

Countries

China

Contacts

Public ContactYangzhiquan

Beijing Zhongguancun Hospital

yangzhiquan80@hotmail.com+86 10 8254 8758

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026