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Clinical effect of intermittent oro-esophageal tube feeding combined with Xuanqiaoliyan decotion in patients with dysphagia after stroke

Clinical effect of intermittent oro-esophageal tube feeding combined with Xuanqiaoliyan decotion in patients with dysphagia after stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046004
Enrollment
Unknown
Registered
2021-05-02
Start date
2018-01-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

stroke

Interventions

experimental group:intermittent oro-esophageal tube feeding (IOE) combined with Xuanqiaoliyan decotion
control group:intermittent oro-esophageal tube feeding (IOE)

Sponsors

Yidu Central Hospital Affiliated Hospital of Weifang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
47 Years to 71 Years

Inclusion criteria

Inclusion criteria: 1. According to the diagnostic criteria of stroke in Chinese guidelines for the prevention and treatment of cerebrovascular diseases; 2. Dysphagia was confirmed by clinical standard swallowing assessment (SSA) and Wadian drinking water test; 3. The patient's condition is stable and conscious, and can cooperate with IOE operation independently and tolerate the treatment of traditional Chinese medicine; 4. Patients with complete clinical data voluntarily participated in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with esophageal tumor and other cardiovascular and cerebrovascular diseases; 2. Autoimmune dysfunction, liver and kidney dysfunction; 3. Patients with mental illness; 4. The patients who did not tolerate the treatment used in this study.

Design outcomes

Primary

MeasureTime frame
standardized swallowing assessment, SSA;

Countries

China

Contacts

Public ContactPanel Haiying

Yidu Central Hospital Affiliated Hospital of Weifang Medical University

515503151@qq.com+86 13780803296

Outcome results

None listed

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