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CLINICAL STUDY · NCT07881107

Preoperative Airway Assessment and Difficult Tracheal Intubation

CompletedNot reportedObservational

Sponsored by Bursa City Hospital

Condition
Difficult Tracheal Intubation, Difficult Laryngoscopy, Difficult Mask Ventilation
Study locations
1 reported site
Study updated
19 Oct 2026
Source
ClinicalTrials.gov

Overall study status is shown above. Individual hospitals may have a different recruitment status.

THE STUDY

About this study

This retrospective observational study examined the association between preoperative airway assessment findings and difficulty placing a breathing tube during general anesthesia. Existing records of 812 adults at Bursa City Hospital were analyzed, including 759 patients with anticipated and 53 with unanticipated airway difficulty. The primary outcome was the need for more than one intubation attempt. No additional procedures were performed for research purposes.
Full official title
Preoperative Airway Assessment Findings Associated With Difficult Tracheal Intubation and Characteristics of Unanticipated Difficult Airway: A Retrospective Cohort Study
Detailed description
Anesthesia records from operations performed between May 2024 and March 2026 were reviewed retrospectively. Seven routinely documented bedside airway assessment findings were evaluated. Associations with difficult intubation, difficult laryngoscopy, Cormack-Lehane grade III-IV, and difficult mask ventilation were analyzed in the anticipated-difficult-airway group, with adjustment for age and sex. Patients with unanticipated airway difficulty were described separately.

PARTICIPATION

Who may participate

Minimum age
18 Years
Maximum age
Not reported
Sex eligibility
All sexes
Healthy volunteers
Not accepted

Only the study team can confirm eligibility. The registry criteria below are not a medical recommendation.

Full inclusion and exclusion criteria
Inclusion Criteria:

* Age 18 years or older.
* General anesthesia with endotracheal intubation at Bursa City Hospital between May 2024 and March 2026.
* Documented anticipated difficult airway before surgery or unanticipated difficult airway during intraoperative airway management.

Exclusion Criteria:

* Patients managed exclusively with regional anesthesia without tracheal intubation.
* Patients managed with a laryngeal mask airway instead of endotracheal intubation.

Study population

Adults undergoing general anesthesia with endotracheal intubation at Bursa City Hospital between May 2024 and March 2026. From a source population of 29,814 intubated adults, the analyzed cohort included 759 patients with anticipated difficult airway and 53 with unanticipated difficult airway, totaling 812 patients.

NEAR YOU

Study locations worldwide

1 site

Check the individual site’s status and contact the listed study team for current availability.

WHAT IS BEING STUDIED

Treatments and study groups

Study groups

Anticipated Difficult AirwayNot reported
Adults with clinician-documented anticipated difficult airway at preoperative assessment who underwent general anesthesia with endotracheal intubation (n=759).
Unanticipated Difficult AirwayNot reported
Adults without documented preoperative suspicion of difficult airway who experienced clinician-documented airway difficulty during general anesthesia with endotracheal intubation (n=53).

RESEARCH DETAILS

Study design

Study type
Observational
Phase
Not reported
Primary purpose
Not reported
Allocation
Not reported
Study model
Cohort
Masking
Not reported
Enrolment
812 participants · Actual
Time perspective
Retrospective

TIMELINE & MEASURES

Dates and outcomes

Study started
25 Feb 2026 · Actual
Primary completion
31 May 2026 · Actual
Study completion
31 May 2026 · Actual
First registered
19 Oct 2026 · Actual
Last registry update
19 Oct 2026 · Actual
Status last verified
Oct 2026
Primary outcomes (1)

Difficult Tracheal Intubation

Proportion of patients requiring more than one tracheal intubation attempt, as documented in anesthesia records.

Time frame: During airway management for the index surgery (day 0).

Secondary outcomes (3)

Difficult Laryngoscopy

Proportion of patients with clinician-documented difficulty during direct or video laryngoscopy.

Time frame: During laryngoscopy for the index surgery (day 0).

Cormack-Lehane Grade III or IV

Proportion of patients with a documented Cormack-Lehane grade III or IV laryngoscopic view.

Time frame: During laryngoscopy for the index surgery (day 0).

Difficult Mask Ventilation

Proportion of patients with clinician-documented difficulty providing adequate face-mask ventilation.

Time frame: During anesthesia induction for the index surgery (day 0).

STUDY TEAM

Sponsor and contacts

Lead sponsor
Bursa City Hospital
Sponsor type
Other gov
Collaborators
Ulusoy, Emre, M.D.
Organisation study ID
bsh0002

Central study contacts

No central contact is currently reported. Check the site contacts or the official record.

Contacts are provided by the registry for study enquiries. Do not use these details for marketing or promotions.

FURTHER READING

Results, documents and references

No results are posted in this registry record

This does not mean the study has no findings. Results may not yet have been submitted or published here.

No study documents are listed in this record.

Source: ClinicalTrials.gov · Data fetched 21 Oct 2026, 16:51 GMT+0530

Registry data timestamp: 2026-10-20T09:00:04

Registry content is reformatted for readability; original study text is not rewritten. Missing information is labelled “Not reported”. Records are supplied by study sponsors or investigators and can change.

ClinicalTrials.gov does not endorse PharmaBharat. Listing a study does not mean it has been evaluated or approved by a government agency. Information is for research awareness and is not medical advice. Data source terms · Registry disclaimer