Dysphagia after ischemic stroke
Conditions
Interventions
Treatment group:Tongliyanqiao acupuncture combined with rTMS
Control group 1:Tongliyanqiao acupuncture
Sponsors
The First Hospital of Hunan University of Chinese Medicine
Eligibility
Sex/Gender
All
Age
40 Years to 80 Years
Inclusion criteria
Inclusion criteria: ? Patients diagnosed by CT or MRI, who meet the above diagnostic criteria of Chinese and Western medicine, and the staging criteria belong to the convalescent stage; ?Age 40-80 years old, gender is not limited; ?WST=2, and VFSS confirmed the presence of pharyngeal dysphagia; ?VFSS score, oral stage 2 to 3 points; ? Stable condition (no progress in symptoms and signs within 48h, stable vital signs), clear consciousness, able to understand basic instructions, no serious cognitive dysfunction, can cooperate with treatment; ? no sequelae such as dysphagia were left after the onset of the disease for the first time or a history of previous stroke, and acupuncture, rehabilitation and other related treatments were not used recently; ? Volunteers to participate in the clinical trial study and cooperate with the examination and treatment, and sign the informed consent. Those who meet the above criteria can be included.
Exclusion criteria
Exclusion criteria: ? Those who do not meet the above diagnostic criteria or inclusion criteria; ?Patients with severe primary diseases such as heart, lung, liver, kidney, rheumatism, immune, endocrine, or heart, lung, liver, kidney, or brain failure; ? Patients with swallowing disorders not caused by the above cerebrovascular accidents; ?Patients with complete aphasia, true bulbar palsy, or speech dysfunction can not cooperate with the scale examination; ? Allergic to contrast agents; ? Women who are pregnant or breastfeeding; ? People with other medical conditions who are using drugs or are receiving treatment that may have an impact on this study indicator; ?Patients who suffer from needle faintness or sustained skin tissue damage, infection, coagulation dysfunction and skin allergy at the acupuncture site; ? Patients have no desire for treatment and are unwilling to cooperate; Patients who refuse to participate in experimental studies; Those meeting any of the above criteria are excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Standardized swallowing assessment; | — |
Secondary
| Measure | Time frame |
|---|---|
| VFSS;Fiberoptic endoscopic evaluation of swallowing;SWAL-QOL;Barthel index; | — |
Countries
China
Contacts
Public ContactLi zhengyu
The First Hospital of Hunan University of Chinese Medicine
Outcome results
None listed