Clinical Trials Directory

Trials / Completed

CompletedNCT00948350

Anesthesia for Awake Fiberoptic Intubation

Anesthesia for Awake Fiberoptic Intubation in Patients With Cervical Instability - Comparison of Translaryngeal Injection and "Spray as You go"-Technique

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Klinikum St. Georg gGmbH · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, comparative, randomized, monocentric, clinical open study, to compare two anesthesia techniques (translaryngeal injection vs. spray as you go) in patients with cervical instability with regard to technical modalities and quality of fiberoptic awake intubation.

Detailed description

In patients with cervical instability anesthesia induction and conventional intubation are associated with the risk of neurological harm. Therefore the method of choice for anesthesia induction is the fiberoptic awake intubation. This method allows to place the ventilation tube without movement of the cervical spinal cord. This procedure is very uncomfortable for the patient and needs the application of topic and/or systemic anesthetics. With this clinical study we will compare two established techniques for local laryngeal anesthesia with regard to the quality of technical modalities and postoperative outcome.

Conditions

Interventions

TypeNameDescription
PROCEDUREawake intubationtwo anesthesia techniques

Timeline

Start date
2009-01-01
Primary completion
2014-01-01
Completion
2014-01-01
First posted
2009-07-29
Last updated
2015-04-20

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00948350. Inclusion in this directory is not an endorsement.