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Post Extubation Dysphagia

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Completed

Conditions

Severity of Aspiration in Post-extubated Subjects

Treatments

Other: Evaluation of Swallowing

Study type

Observational

Funder types

Other

Identifiers

NCT01849679
2012-0407

Details and patient eligibility

About

The investigators hypothesize that aspiration will be more prevalent at two to four hours post-extubation but will resolve in the majority of patients by 24 to 26 hours post-extubation.

The purpose of the research is to investigate whether there is a difference in swallow function two to four hours after extubation (removal of breathing tube) compared to 24 hours after extubation. This information will help healthcare providers decide if it is necessary for people to wait 24 hours after extubation before they start eating and drinking.

Enrollment

71 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients that were intubated for more than 48 hours.
  • Adults, 18 and over
  • All races
  • Males and females
  • Approval to participate in the study by the treating physician

Exclusion criteria

  • Patients with a history of oropharyngeal dysphagia.
  • Patients with neurological disorders associated with dysphagia including dementia, Parkinson's disease, multiple sclerosis, stroke, and ALS.
  • Patients with a history of head and neck cancer or laryngeal surgery.
  • Patients that are not candidate for FEES because of facial fractures, nothing by mouth (NPO) status for other procedures, elevated bleeding risk (patients on therapeutically dosed anticoagulant infusion or injection, platelet count less than 50,000, INR greater than 2.0, partial thromboplastin time greater than 1.5 times normal), decreased level of arousal/alertness, significant agitation, or inability to tolerate room air or nasal cannula oxygen for duration of FEES.
  • Patients who are extubated after 1400 or on weekends (Friday, Saturday, or Sunday).
  • Non-English Speakers will be excluded

Trial design

71 participants in 1 patient group

Post-Extubation Subjects
Treatment:
Other: Evaluation of Swallowing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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