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A quasi-experimental study of graded rehabilitation strategies for patients with Post-extubation dysphagia in ICU

Construction and preliminary application of a graded rehabilitation program for swallowing function in patients with dysphagia after tracheal intubation and extubation in ICUs

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089264
Enrollment
Unknown
Registered
2024-09-04
Start date
2024-06-10
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

Dysphagia after tracheal intubation extubation

Interventions

intervention group :Swallowing function graded rehabilitation program
control group :Routine care and routine swallowing rehabilitation

Sponsors

The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Age =18 in ICU; (2) Patients who underwent mechanical ventilation and successfully removed the tracheal intubation, and had PED after SSA (> 18 points) assessment within 4 to 6 hours after extubation; (3) Can understand and cooperate with the execution of simple instructions; (4) The patient agreed to participate in the study.

Exclusion criteria

Exclusion criteria: (1) Patients with tracheotomy; (2) Patients with water fasting after tracheal intubation and extubation; (3) Abnormal neurological and oropharyngeal functions, such as neuromuscular diseases, cerebrovascular diseases, cervical pharyngeal surgery, vocal cord function abnormalities, etc.; (4) Patients with aspiration pneumonia; (5) Previous dysphagia.

Design outcomes

Primary

MeasureTime frame
swallowing function;

Secondary

MeasureTime frame
Function of swallowing muscle;Changes in blood oxygen saturation;Incidence of cough;

Countries

China

Contacts

Public ContactWang Yuyu

The First Affiliated Hospital of Soochow University

wangyuyu0908@163.com+86 139 6251 6015

Outcome results

None listed

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