ClinicalTrials.Veeva

Menu

Comparison of Two Different Types of "Spray as You go" Technique for Awake Fiberoptic Intubation

J

Johannes Gutenberg University (JGU)

Status

Completed

Conditions

Awake Fiberoptic Intubation

Treatments

Device: bronchoscope
Device: Enk Fiberoptic Atomizer

Study type

Interventional

Funder types

Other

Identifiers

NCT01995292
Atomizer1.0

Details and patient eligibility

About

The purpose of this study is to determine whether modified "spray as you go" technique using the Enk Fiberoptic Atomizer Set during awake fiberoptic intubation is more comfortable for the patient.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18 years
  • no concurrent participation in another clinical trial
  • German language in speaking and writing
  • Capability of giving consent
  • written informed consent
  • an elective surgery under general anesthesia, in which an awake fiberoptic intubation is indicated

Exclusion criteria

  • Age < 18 years
  • pregnant women
  • patients unwilling or unable to give informed consent
  • ASA classification > 3
  • Known allergy to local anesthetics
  • Participation in another clinical trial

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

bronchoscope
Experimental group
Description:
Patients will receive local anaesthetics via the working channel of the bronchoscope.
Treatment:
Device: bronchoscope
Enk Fiberoptic Atomizer
Experimental group
Description:
Patients will receive local anaesthetics for the awake fiberoptic intubation via the Enk Fiberoptic Atomizer.
Treatment:
Device: Enk Fiberoptic Atomizer

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems