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A new type of balloon catheter-based dilatation intervention for patients with dysphagia after stroke: a randomized controlled trial

new type of balloon catheter-based dilatation intervention for patients with dysphagia after stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044034
Enrollment
Unknown
Registered
2021-03-08
Start date
2019-02-05
Completion date
Unknown
Last updated
2021-07-21

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

Conditions

dysphagia after stroke

Interventions

experimental group:dilatation intervention using the new type balloon catheter
control group:the ordinary urinary catheter

Sponsors

Hunan Provincial People's Hospital (The First Affiliated Hospital of Hunan Normal University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. having a diagnosis of cricopharyngeus achalasia confirmed by the video fluoroscopy swallowing study or clinical swallowing evaluation; 2. Radiologists confirmed stroke by head Magnetic Resonance Imaging; 3. being aged 20 -80 years; 4. willing to participated the study.

Exclusion criteria

Exclusion criteria: 1) Organic obstruction of nasal or pharyngeal; 2) sever heart, lung and kidney diseases; 3) mental illness; 4) severe cognitive disorder and aphasia.

Design outcomes

Primary

MeasureTime frame
duration for intervention;—

Secondary

MeasureTime frame
recovery time of oral feeding water and other foods (liquid food, mushy food and solid food);duration for FOIS score of 3 or more;EAT-10 score at the termination;—

Countries

China

Contacts

Public ContactHu Tingting

Hu'nan Provincial People's Hospital (The First Affiliated Hospital of Hunan Normal University)

494727666@qq.com+86 15874028534

Outcome results

None listed

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