MedTrace Logo

Anesthesia for Awake Fiberoptic Intubation

NCT00948350 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2015-04-20

No results posted yet for this study

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.

Conditions

  • Intubation

Interventions

PROCEDURE

awake intubation

two anesthesia techniques

Sponsors & Collaborators

  • Klinikum St. Georg gGmbH

    lead OTHER

Principal Investigators

  • Armin R Sablotzki, MD · Clinics of Anesthesiology, Critical care and Pain Therapy

  • Michael Malcharek, MD · Clinic of Anesthesiology, Dept. Neuroanesthesia and Neuromonitoring

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2014-01-31
Completion
2014-01-31

Countries

  • Germany

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00948350 on ClinicalTrials.gov