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Not yet recruitingNCT07355608VIDIGLOVUpdated Aug 11, 2026

Videolaryngoscopic Difficult ıntubation and Glottic View Score: A Multicentre Prospective Study

An observational study in Airway Management, sponsored by Diskapi Teaching and Research Hospital. Not yet recruiting at 2 sites in Turkey (Türkiye). Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2026-08-11.

Sponsored by Diskapi Teaching and Research Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
4,977
Ages
18 Years to 100 Years
Sex
All
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Study summary

Background:

Videolaryngoscopy has improved glottic visualization and facilitated tracheal intubation. However, difficulties-including failed intubation-still occur. At present, no prospectively derived classification system exists to assess the difficulty of videolaryngoscopic (VL) intubation across both normal and anticipated difficult airways. Additionally, current glottic view grading systems, designed for direct laryngoscopy, may not adequately capture the specific challenges of VL intubation.

Objectives:

This study aims to:

  1. Develop a predictive model for difficult VL intubation in surgical patients with both normal and anticipated difficult airways.
  2. Create a glottic view scoring system specifically tailored to videolaryngoscopy.
  3. Compare the predictive accuracy of the new scoring system with existing laryngeal view grades in forecasting difficult VL intubation.
Read the detailed description

Background:

Videolaryngoscopy has improved glottic visualization and facilitated tracheal intubation. However, difficulties-including failed intubation-still occur. At present, no prospectively derived classification system exists to assess the difficulty of videolaryngoscopic (VL) intubation across both normal and anticipated difficult airways. Additionally, current glottic view grading systems, designed for direct laryngoscopy, may not adequately capture the specific challenges of VL intubation.

Objectives:

This study aims to:

  1. Develop a predictive model for difficult VL intubation in surgical patients with both normal and anticipated difficult airways.
  2. Create a glottic view scoring system specifically tailored to videolaryngoscopy.
  3. Compare the predictive accuracy of the new scoring system with existing laryngeal view grades in forecasting difficult VL intubation.

Methods:

A prospective cohort of 4,977 patients will be enrolled. Patient and intubation related variables-including VL findings, airway features, clinical parameters, device, and procedural details-will be analyzed. Binary logistic regression will be employed to build the initial predictive model. In parallel, machine learning techniques (Random Forest, Support Vector Machine, XGBoost, LightGBM, etc.) will be applied to evaluate predictive performance. Comparative analysis will be conducted between the machine learning models and the logistic regression baseline.

Expected Impact:

The development of a robust predictive tool and an associated VL-specific glottic view score could enhance clinical decision making, particularly in identifying patients at risk of difficult or failed VL intubation. This may support early consideration of awake tracheal intubation, and use of standardized terminology and reduce complications associated with difficult airway management

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Conditions studied

  • Airway Management

Keywords

  • Airway management
  • Videolaryngoscope
  • Difficult airway
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In context

Lead sponsor

Diskapi Teaching and Research Hospital is the lead sponsor of 106 studies on the registry; 13 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 to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Adults, both with normal or predicted difficult airways, undergoing orotracheal intubation with a videolarygoscope, for a case mix of surgeries

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

  • Adults
  • Both with normal or predicted difficult airways
  • Undergoing orotracheal intubation with a videolarygoscope

Exclusion criteria

Exclusion Criteria:

  • Rapid sequence intubation
  • Double lumen tube intubation
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
4,977 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Failed first intubation attempt

    Failed to intubate at firtst attempt

    Time frame: 2 minutes after anesthesia induction

  2. Difficult intubation

    Failed to intubate at 1-2 attempts and/or intubation duration longer than 120 second

    Time frame: 2 minutes after anesthesia induction

  3. Failed intubation

    Not able to intubate the patient

    Time frame: 2 minutes after anesthesia induction

  4. Intubation duration

    Time elapsed from entring the blade between the teeth to detecting an entidal carbondioxide trace

    Time frame: 2 minutes after anesthesia induction

  5. Glottic view description

    Vocal cords are fully visible Vocal cords are partially separately Vocal cords are not visible Cords are adducted Epiglottis is visible Epiglottis is large Epiglottis is small Epiglottis is edematous Epiglottis mass is present Arytenoids are visible Arytenoid luxation or subluxation Arytenoid edema Valecula problem (edema, Coffee grounds, etc., unable to insert a blade) Aryepiglottic plica pathology (edema, Coffee grounds scar) Laryngeal structures should be formed Glottic stenosis Laryngospasm

    Time frame: 2 minutes after anesthesia induction

Secondary outcomes

  1. Percentil of glottic opening score

    the percentage of glottic opening seen, defined by the linear span from the anterior commissure to the inter-arytenoid notch

    Time frame: 2 minutes after anesthesia induction

  2. Cormack lehanne score

    grade 1 being a full view of the glottis, grade 2 being a partial view, grade 3 being only a view of the epiglottis, and grade 4 being an absent view of the glottis and epiglottis

    Time frame: 2 minutes after anesthesia induction

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Study locations

2 sites
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References and documents

Publications

  • Xia M, Jin C, Zheng Y, Wang J, Zhao M, Cao S, Xu T, Pei B, Irwin MG, Lin Z, Jiang H. Deep learning-based facial analysis for predicting difficult videolaryngoscopy: a feasibility study. Anaesthesia. 2024 Apr;79(4):399-409. doi: 10.1111/anae.16194. Epub 2023 Dec 13. PubMed 38093485 ↗
  • O'Loughlin EJ, Swann AD, English JD, Ramadas R. Accuracy, intra- and inter-rater reliability of three scoring systems for the glottic view at videolaryngoscopy. Anaesthesia. 2017 Jul;72(7):835-839. doi: 10.1111/anae.13837. Epub 2017 Mar 24. PubMed 28337769 ↗

Individual participant data

Plan to share: No

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2026; primary completion for Feb 2027, 4 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 2, 2025
First posted
Jan 21, 2026
StartEst.
Oct 1, 2026
Primary completionEst.
Feb 1, 2027
CompletionEst.
Feb 1, 2027
Last update
Aug 11, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 11, 2026, 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
NCT07355608
Responsible party
DILEK YAZICIOGLU (Professor of Anesthesiology, Diskapi Teaching and Research Hospital) — Principal investigator
First posted
Jan 21, 2026
Start date
Oct 1, 2026 (estimated)
Primary completion
Feb 1, 2027 (estimated)
Completion
Feb 1, 2027 (estimated)
Last update
Aug 11, 2026

Study contacts

Dilek Yazıcıoğlu Ünal, Professor
Contact
dilekunalmd@gmail.com
+90 5336957855
Emel Gündüz, assoc.
Contact
dregunduz@hotmail.com,
+905444341719
Dilek Yazıcıoğlu Ünal, professor
principal investigator · Ankara Etlik City Hospital

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 not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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