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CompletedNCT02613429Updated Jan 5, 2016

Identification of Airway Structures Necessary for Airway Access Via the Skin

An interventional study of identification of the airway by from the cranial end and identification of the airway from the distal end in Upper Airway Obstruction, sponsored by Rigshospitalet, Denmark. Completed at 2 sites in Denmark. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-01-05.

Sponsored by Rigshospitalet, Denmark · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

Literature shows that anaesthetists have a low success-rate when trying to access the airway percutaneously in case of failed ventilation and intubation.

The study will investigate anaesthetists ability to locate the trachea and the thyroid cartilage and the cricoid cartilage in patients, using different methods including application of ultrasonography.

Read the detailed description

Literature shows that anaesthetists have a low success-rate when trying to access the airway percutaneously in case of failed ventilation and intubation.

The researchers will investigate anaesthetists ability to locate the trachea and the thyroid cartilage and the cricoid cartilage of a healthy subject with different methods including application of ultrasonography.

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Conditions studied

  • Upper Airway Obstruction

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03

In context

Airway Obstruction

154 studies on the registry are indexed under Airway Obstruction; 30 are open to participants now.

This study's enrollment of 42 is below the median of 56 across 92 interventional studies indexed under Airway Obstruction.

Browse Airway Obstruction studies →

Lead sponsor

Rigshospitalet, Denmark is the lead sponsor of 1,017 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Anaesthesiologist

Exclusion criteria

Exclusion Criteria:

  • unvillingnes to participate
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
42 participants (actual)

Study arms

  • Active comparator
    Cranial horizontal

    identification of the airway by from the cranial end. Marking of the airway, including the cricothyroid membrane, on the skin, by starting the examination from the cranial end at the level of the thyroid catilage , horizontally and thereafter moving caudally

    Behavioral: identification of the airway by from the cranial end

  • Active comparator
    caudal longitudinal

    identification of the airway from the distal end. Marking of the airway, including the cricothyroid membrane, on the skin, by starting the examination caudally, and then moving cranially

    Behavioral: identification of the airway from the distal end

Interventions

  • Behavioralidentification of the airway by from the cranial end

    The airway is identified with inspection and imaging technique (ultrasound) by placing the ultrasound transducer over the thyroid cartilage and from there moving distally

  • Behavioralidentification of the airway from the distal end

    The airway is identified with inspection and imaging technique (ultrasound) by placing the ultrasound transducer over the distal trachea and moving cranially

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What researchers measure

Primary outcomes

  1. time to identify the structures necessary for percutaneous airway acess

    Time frame: two minutes after initiation of the attempt to identify the airway structures

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Study locations

2 sites
  • Rigshospitalet, department of anaesthesia
    Copenhagen, 2000, Denmark
  • Rigshospitalet, section for anaesthesia for ENT and Maxillofacial surgery, section 3071
    Copenhagen, 2100, Denmark
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 5, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02613429
Lead sponsor
Rigshospitalet, Denmark
Responsible party
Michael Seltz Kristensen (Head of clinical anaesthesia and research, ENT and max fax, Rigshospitalet, Denmark) — Principal investigator
First posted
Nov 24, 2015
Start date
Nov 2015
Primary completion
Dec 2015
Completion
Dec 2015
Last update
Jan 5, 2016

Study contacts

Michael S Kristensen, M.D.
study chair · Rigshospitalet, Denmark

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2016. You cannot join it, but the record below documents what was studied.

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