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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | awake intubation | two 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.