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NCT Number: NCT04575870

Return of Aspiration-Free Swallow After Laryngotracheal Anesthesia

Patients undergo laryngotracheal anesthesia (LTA) for a variety of in-office laryngology procedures. Prior to resolution of laryngeal sensory anesthesia, oral intake may predispose patients to aspiration. The purpose of this study is to objectively characterize a time period for return of aspiration-free swallow after LTA.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Alabama at Birmingham

Birmingham, Alabama, 35233, United States

About this study

Swallowing is a complex process involving coordination of multiple muscle groups. Sensation in the throat is very important for swallowing safely. Laryngotracheal anesthetic (LTA, or topical application of lidocaine anesthetic to larynx and trachea) is needed for a variety of in-office laryngology procedures, including examination of the air passage, or tracheobronchoscopy. This causes a temporary decrease in sensation that can affect swallow function and result in aspiration (passage of swallowed material into lungs instead of into esophagus and stomach). It is not known how long this effect lasts. It would be helpful to know this for counseling patients on when they can resume swallowing after a procedure. In general, most patients are advised to avoid eating/drinking for 90 minutes after their procedure to allow for sensation to return. To date, there has been no study characterizing the time required for return of aspiration-free swallow after LTA.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 years or older
  • Ability of patients to speak and understand English
  • Ability for patients to consent for themselves
  • Undergoing tracheobronchoscopy procedure for the treatment of airway stenosis
  • Eating Assessment Tool (EAT-10) score ≤ 3

Exclusion criteria

  • Age less than 18 years
  • Patients unable or unwilling to provide informed consent
  • Women who are pregnant
  • History of abnormal swallowing evaluation, either videofluroscopic study of swallow or functional endoscopic evaluation of swallowing (FEES)
  • History of medical condition affecting swallowing, such as
  • Neurodegenerative disorders: stroke, traumatic brain injury, dementia, motor neuron disease, myasthenia gravis, cerebral palsy, Gullain-Barre syndrome, poliomyelitis, myopathy, Parksonism, Huntingon's disease, progressive supranuclear palsy, Wilson's disease, vocal fold paralysis
  • Connective tissue disorders: polymyositis, dermatomyositis, progressive systemic sclerosis, Sjogren's disease, scleroderma
  • History of gastroesophageal tumor
  • History of gastroesophageal surgery
  • History of recent open central neck surgery (i.e., thyroidectomy, anterior cervical discectomy or fusion)
  • History of head and neck cancer
  • History of head and neck radiation therapy or chemotherapy

Treatment and study plan

Waiting Period

Other

amount of time between clinical procedure and modified functional endoscopic exam of swallowing

Primary outcomes

  1. Modified functional endoscopic exam of swallowing (FEES)

    Time frame: Up to 90 minutes

    A modified functional endoscopic exam of swallowing (FEES) is an examination where a small amount of water will be ingested. Each subject will perform about three water swallows. Water will be dyed with green food coloring to facilitate visualization, as is standard with the FEES procedure. If the water passes normally to the esophagus, this will be considered a pass; if the water is aspirated, this will be considered a fail.

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Registry information

Official study title

Return of Aspiration-Free Swallow After Laryngotracheal Anesthesia (LTA)

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Oct 5, 2020
Registry last updated
Apr 24, 2024

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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