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

Phase 1

Recruiting

• Conditions: Dysphagia after stroke

• Registration Number: ITMCTR2100004432
• Lead Sponsor: The Second Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: Not specified

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

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.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
VFSS;Dynamic laryngoscope;Swallowing scale;Swallow surface electromyography;

Secondary Outcome Measures

Name	Time	Method
rs-fMRI;