ClinicalTrials.gg
CompletedNCT03480035Updated Dec 21, 2018

Ideal Point of Transluminal Light in Tracheal Intubation With a Light Wand

An observational study in Neck Disease, Trismus and Tooth Abnormalities, sponsored by Keimyung University Dongsan Medical Center. Completed at 1 site in Korea, Republic of. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-12-21.

Sponsored by Keimyung University Dongsan Medical Center · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
107
Ages
18 Years and older
Sex
All
01

Study summary

If the patients's teeth are weak or the mouth dose not open well, the lightwand is a useful device when endotracheal intubation is necessary.

Therefore, if the appropriate position of the light beam is determined and the distance of the light source suitable for intubation using the lightwand is obtained from anatomical structures such as thyroid cartilage and cricoid cartilage, it is clinically useful. Because it can prevent unnecessary deep insertion or shallow insertion that can cause damage to anatomical structures during intubation.

Read the detailed description

Studies have been reported on the proper position to bend the lightwand and the appropriate angle to bend when performing endotracheal intubation with lightwand. For ease of procedure, the assistant has to lift the patient's lower jaw or perform a neck extension.

However, there is no report on the position of the lightbulb when the light passes through the front of the airway and neck and appears bright in the midpoint.

The prodcedure is as follows.

  1. FOB examination and check position of light below 1cm from vocal cord
  2. lightwand intubation aimed at checkpoint
  3. measurement of distance from thyroid cartilage/cricoid cartilage to light point
02

Conditions studied

  • Neck Disease
  • Trismus
  • Tooth Abnormalities

Browse trials for

03

In context

Trismus

107 studies on the registry are indexed under Trismus; 19 are open to participants now.

Browse Trismus studies →

Lead sponsor

Keimyung University Dongsan Medical Center is the lead sponsor of 86 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

This is an adult patient who is 18 years of age or older who undergoes general anesthesia requiring intubation.

Among them, patients who are unable to extend their necks, have trismus or have weak teeth are selected.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • impossibility of neck extension
  • trismus
  • weak teeth

Exclusion criteria

Exclusion Criteria:

  • previous history of larynx or neck surgery
  • no
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
107 participants (actual)
Patient registry
No

Interventions

  • Procedurelightwand intubation

    intubation using lightwand

06

What researchers measure

Primary outcomes

  1. distance from lightbeam of the FOB to thyroid cartilage

    we will measure straight distance from lightbeam of the FOB to thyroid cartilage on the surface of patient's neck

    Time frame: before intubation

  2. distance from lightbeam of the FOB to cricoid cartilage

    we will measure straight distance from lightbeam of the FOB to cricoid cartilage on the surface of patient's neck

    Time frame: before intubation

Secondary outcomes

  1. distance from lightbeam of the FOB to sternal notch

    we will measure straight distance from lightbeam of the FOB to sternal notch on the surface of patient's neck

    Time frame: before intubation

07

Study locations

1 site
  • Dongsan medical center
    Daegu, Korea, Republic of
08

References and documents

Publications

  • Cho E, Kim HC, Lee JM, Park JH, Ha N, Hong JH, Lee J. Evaluation of transmitted glow point at a priori chosen depth (1 cm below vocal cords) for lightwand intubation: a prospective observational study. J Int Med Res. 2020 Dec;48(12):300060520974249. doi: 10.1177/0300060520974249. PubMed 33284717 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 21, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03480035
Lead sponsor
Keimyung University Dongsan Medical Center
Responsible party
Jiwon Lee (assistant professor, Keimyung University Dongsan Medical Center) — Principal investigator
First posted
Mar 27, 2018
Start date
Mar 6, 2018
Primary completion
Jul 27, 2018
Completion
Jul 27, 2018
Last update
Dec 21, 2018

Study contacts

Jiwon Lee, Dr.
principal investigator · Dongsan Medical Center

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion