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Post-extubation Assessment of Laryngeal Symptoms and Severity (PALSS)

Johns Hopkins University logo

Johns Hopkins University

Status

Completed

Conditions

Intubation, Intratracheal
Mechanical Ventilation Complication
Critical Illness
Complication of Ventilation Therapy

Treatments

Diagnostic Test: laryngoscopy

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT03726086
IRB00151643
R01NR017433-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this study is to learn more about voice and airway problems that patients experience during and after the time patients have an oral endotracheal tube in patients' airway to help patients breathe while receiving mechanical ventilation in an intensive care unit (ICU).

Enrollment

365 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥18 years old
  • Required mechanical ventilation via an oral endotracheal tube
  • Anticipated intubation ≥8 hours

Exclusion criteria

  • Pre-existing dysphonia, dysphagia
  • Pre-existing central nervous system, neuromuscular, or connective tissue disease
  • Prior tracheotomy and/or tracheotomy placed prior to enrollment
  • History of major thoracic surgery (e.g., sternotomy, thoracotomy) prior to the current admission
  • Head and/or neck disease
  • Head and/or neck surgery other than tonsillectomy
  • Known or suspected anatomical abnormalities or pre-intubation trauma of the oral cavity, pharynx, larynx, or esophagus
  • Unlikely to be extubated (i.e., expected death)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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