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Swallowing Disorders After Prolonged Mechanical Ventilation

Current Care Study of Incidence and Consequences of Swallowing Disorders After Invasive Mechanical Ventilation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01360580
Acronym
Deglutube
Enrollment
138
Registered
2011-05-25
Start date
2011-01-31
Completion date
2012-12-31
Last updated
2013-01-24

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

Conditions

Larynx Disease

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?)

Interventions

None listed

Sponsors

University Hospital, Rouen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Prevalence of swallowing disorders after prolonged invasive ventilation48 hours after extubation

Secondary

MeasureTime frame
Nutritional status at day 28day 28

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026