NCT07547943

Brief Summary

This prospective observational study aims to evaluate the predictive value of thyromental height (TMH) and ultrasonographic airway measurements in predicting difficult airway in adult patients undergoing elective surgery under general anesthesia. Preoperative airway assessment will include standard clinical evaluation, TMH measurement, and ultrasonographic measurements of anterior neck soft tissue. Perioperative airway management data, including intubation difficulty, number of attempts, and Cormack-Lehane classification, will be recorded. The relationship between preoperative measurements and difficult airway will be analyzed to determine their predictive accuracy and clinical usefulness.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
240

participants targeted

Target at P75+ for all trials

Timeline
12mo left

Started May 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 13, 2026

Completed
10 days until next milestone

First Posted

Study publicly available on registry

April 23, 2026

Completed
22 days until next milestone

Study Start

First participant enrolled

May 15, 2026

Expected
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2027

Last Updated

April 23, 2026

Status Verified

March 1, 2026

Enrollment Period

1 year

First QC Date

April 13, 2026

Last Update Submit

April 17, 2026

Conditions

Keywords

Thyromental HeightAirway UltrasoundDifficult IntubationCormack-Lehane

Outcome Measures

Primary Outcomes (1)

  • Prediction of Difficult Intubation

    The primary outcome is the ability of thyromental height (TMH) and ultrasonographic airway measurements to predict difficult intubation. Difficult intubation will be defined as Cormack-Lehane grade ≥3, requirement of multiple intubation attempts, or use of advanced airway devices.

    During induction of anesthesia (intraoperative period)

Study Arms (1)

Airway Assessment Cohort

Adult patients undergoing elective surgery under general anesthesia will be included. All participants will undergo standard preoperative airway assessment, including thyromental height (TMH) measurement and ultrasonographic airway evaluation. Intraoperative airway management and intubation-related parameters will be recorded to assess the predictive value of TMH and ultrasound measurements for difficult airway.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients undergoing elective surgical procedures under general anesthesia at a tertiary care hospital will be prospectively enrolled. All participants will undergo standardized preoperative airway assessment, including thyromental height measurement and ultrasonographic airway evaluation, followed by perioperative airway management assessment.

You may qualify if:

  • Adult patients aged 18 years and older Patients scheduled for elective surgery under general anesthesia Patients requiring endotracheal intubation Patients who provide written informed consent

You may not qualify if:

  • Patients with known upper airway pathology (e.g., tumor, trauma, infection) Patients with previous head and neck surgery or anatomical deformity affecting airway evaluation Patients with limited mouth opening (\<3 cm) or severe cervical spine restriction Patients with contraindications to ultrasonographic examination Patients requiring rapid sequence induction or emergency surgery Patients who refuse to participate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bursa City Hospital

Bursa, Nilüfer, 16110, Turkey (Türkiye)

Location

Central Study Contacts

Serra Topal, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD

Study Record Dates

First Submitted

April 13, 2026

First Posted

April 23, 2026

Study Start (Estimated)

May 15, 2026

Primary Completion (Estimated)

May 15, 2027

Study Completion (Estimated)

May 15, 2027

Last Updated

April 23, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared due to institutional policies and protection of patient confidentiality.

Locations