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Comparison of rTMS and iTBS in the treatment of dysphagia after stroke: A prospective, blind, randomized controlled study

Multimodal functional evaluation of different non-invasive brain regulation techniques for dysphagia after stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058246
Enrollment
Unknown
Registered
2022-04-03
Start date
2022-04-05
Completion date
Unknown
Last updated
2023-12-10

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

Conditions

stroke

Interventions

Group 1 :Repeat transcranial magnetic stimulation
Group 2:Intermittent Theta rhythm stimulation
Group 3:Conventional control + rTMS sham stimulation

Sponsors

Yuebei People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. First onset of stroke confirmed by head CT or MRI imaging scan; 2. The course of disease is 2 weeks and 3 months; 3. Stable condition after stroke; 4. Aged 18-85 years; 5. Dysphagia was confirmed after swallowing evaluation by a professional (fiberoptic laryngoscopy swallowing angiography or drinking water test, etc.); 6. Clear consciousness, good cardiopulmonary function, stable vital signs and good coordination with training; 7. Promise to abide by the research procedures, cooperate with the implementation of the whole process of research and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe hypertension (systolic blood pressure > 200 mmHg, diastolic blood pressure > 110 mmHg), diabetes with poor blood sugar control or complicated with serious diseases such as liver, kidney, heart and other important organ dysfunction; 2. There are tumors of the head and neck, local lesions of the throat and esophagus, and abnormal swallowing function of the esophagus; 3. A history of chronic alcoholism or chronic use of central nervous system active drugs; 4. Built-in cardiac pacemaker or other metal medical devices implanted in the body; 5. Severely impaired in vision, hearing or understanding; 6. Pregnant or lactating women; 7. Any condition which, in the opinion of the investigator, is likely to prejudice the subject or cause the subject to be unable to meet or perform the study requirements.

Design outcomes

Primary

MeasureTime frame
Fiberoptic Endoscopic Dysphagia Severity Scale, FEDSS;Rosenbek Penetration/Aspiration Scale , PAS;

Secondary

MeasureTime frame
Standardized Swallowing Assessment, SSA;

Countries

China

Contacts

Public ContactHuiyu Liu

Yuebei People's Hospital

liuhuiyudoctor@sohu.com+86 13922599818

Outcome results

None listed

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