Swallowing Disorders After Prolonged Mechanical Ventilation

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?)

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Key information

Conditions

Larynx Disease Laryngeal Diseases Otorhinolaryngologic Diseases Respiratory Tract Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Service de Réanimation Médicale, Angers, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

Prevalence of swallowing disorders after prolonged invasive ventilation

Time frame: 48 hours after extubation

Secondary outcomes

Nutritional status at day 28

Time frame: day 28

Sponsors and collaborators

Lead sponsor

University Hospital, Rouen

Other

Registry information

Official study title

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

Acronym: Deglutube

Important dates

Study start: 2011
Primary completion: 2012
Study completion: 2012
First posted: May 25, 2011
Registry last updated: Jan 24, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Completed