MedPath

Swallowing Disorders After Prolonged Mechanical Ventilation

Completed
Conditions
Larynx Disease
Registration Number
NCT01360580
Lead Sponsor
University Hospital, Rouen
Brief Summary

Epidemiology study for evaluation of incidence of swallowing disorders (SD) after prolonged invasive ventilation (more than seven days), using a clinical statement. All consecutive patients are screened, and clinical evaluation is performed during 48h after patient's extubation. If a SD exist, a new evaluation is realized 48h after. Three groups will be created (1.no SD, 2.transitory SD and 3.persistent SD (eg persistent after 48h)). Data complementary are notified at day 28 (pneumonia? nutritional status?)

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
138
Inclusion Criteria
  • More than 7 days of invasive mechanical ventilation
Exclusion Criteria
  • Age < 18 years old
  • Preexistent swallowing disorders, stroke, tracheostomy
  • Failure of patient's agreement

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Prevalence of swallowing disorders after prolonged invasive ventilation48 hours after extubation
Secondary Outcome Measures
NameTimeMethod
Nutritional status at day 28day 28

Trial Locations

Locations (2)

Service de Réanimation Médicale

🇫🇷

Angers, France

service de Réanimation médicale

🇫🇷

Rouen, France

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