Clinical Trials Directory

Trials / Terminated

TerminatedNCT01848548

Superior Laryngeal Nerve Block For Awake Endotracheal Intubation Study

Superior Laryngeal Nerve Block For Airway Anesthesia Efficacy Study

Status
Terminated
Phase
Study type
Observational
Enrollment
25 (actual)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Awake tracheal intubation is the standard management for patients as risk for airway compromise. It is also commonly done in cases where there is significant cervical spine pathology i.e. cervical myelopathy or instability. The anesthetic technique used for the awake intubation is crucial to the patient's safety. One of the most important aspects of the anesthetic technique is airway anesthesia prior to placement of an endotracheal tube. The superior laryngeal nerve is responsible for mediating the cough reflex around the vocal cords. The investigators have developed an approach to reliably block the superior laryngeal nerve by injecting local anesthetic near the nerve in a unique approach. Injecting local anesthetic into or through the thyrohyoid membrane will effectively block the superior laryngeal nerve

Conditions

Interventions

TypeNameDescription
PROCEDURESuperior Laryngeal Nerve Block using the Thyrohyoid Membrane as an Anatomic LandmarkThe needle is introduced just lateral to midline above the thyroid notch in a slightly medial direction so as to enter the thyrohyoid membrane, and inserted about 1-1.5 cm. Three milliliters of 2% lidocaine is injected.

Timeline

Start date
2013-04-01
Primary completion
2017-07-01
Completion
2017-07-01
First posted
2013-05-07
Last updated
2017-11-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01848548. Inclusion in this directory is not an endorsement.