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Clinical and basic research on mechanism of 'penetrating needling and swallowing acupuncture' in treating dysphagia after stroke

Clinical and basic research on mechanism of 'penetrating needling and swallowing acupuncture' in treating dysphagia after stroke

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100004432
Enrollment
Unknown
Registered
2020-11-06
Start date
2020-10-27
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Dysphagia after stroke

Interventions

Sponsors

The Second Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients meeting the diagnostic criteria of stroke; 2. Patients with dysphagia showed by VFSS after swallowing angiography; 3. Subjects with limited diet and oral feeding scale score less than or equal to grade v. subjects with Wadian drinking water score above grade III; 4. The subjects with MMSE score of 24 or above can understand and execute the simple instructions of the treatment personnel, and their cognitive ability is acceptable, and they can cooperate with those who are willing to accept the examination and treatment; 5. Subjects aged between 40 and 65 years, regardless of gender; 6. Patients whose course of disease is within 180 days; 7. Patients with clear mind and stable vital signs; 8. Patients who voluntarily participated in the study and signed the informed consent; 9. Patients without serious complications can receive acupuncture treatment and have good compliance.

Exclusion criteria

Exclusion criteria: 1. Subjects with dysphagia not caused by stroke; 2. Pregnant or lactating women; 3. Patients with severe primary chronic diseases such as heart, liver, kidney, hematopoietic system and endocrine system, severe dementia, severe language comprehension disorder and psychosis; 4. Patients with various bleeding tendency diseases; 5. Patients who could not judge the curative effect or the data were incomplete, which affected the curative effect judgment and were not suitable for clinical observation.

Design outcomes

Primary

MeasureTime frame
VFSS;Dynamic laryngoscope;Swallowing scale;Swallow surface electromyography;

Secondary

MeasureTime frame
rs-fMRI;

Countries

China

Contacts

Public ContactXiaoning Li

The Second Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine

lixiaoning456@163.com+86 13313699268

Outcome results

None listed

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