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Clinical Trials/NCT01848548
NCT01848548
Terminated
Not Applicable

Superior Laryngeal Nerve Block For Airway Anesthesia Efficacy Study

Wake Forest University Health Sciences1 site in 1 country25 target enrollmentApril 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Awake Endotracheal Intubation
Sponsor
Wake Forest University Health Sciences
Enrollment
25
Locations
1
Primary Endpoint
The primary outcome measure is to assess the efficacy of blocking the superior laryngeal nerve by using cough at the vocal cords on a 4 point scale
Status
Terminated
Last Updated
8 years ago

Overview

Brief 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

Registry
clinicaltrials.gov
Start Date
April 2013
End Date
July 2017
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

The primary outcome measure is to assess the efficacy of blocking the superior laryngeal nerve by using cough at the vocal cords on a 4 point scale

Time Frame: Immediate Perioperative period

Secondary Outcomes

  • Time to placement of block(Immediate Perioperative Period)

Study Sites (1)

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