NCT06700265

Brief Summary

the goal of the observational study to measure the effectiveness of neck ultrasound in prediction of difficult intubation in adult patients

Trial Health

87
On Track

Trial Health Score

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

Enrollment
246

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2023

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 20, 2023

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

November 11, 2024

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 21, 2024

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2026

Completed
Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

3 years

First QC Date

November 11, 2024

Last Update Submit

April 27, 2026

Conditions

Keywords

airway ultrasound

Outcome Measures

Primary Outcomes (1)

  • measurement of effectiveness of neck ultrasound use of ultrasound measurement in prediction of difficult intubation

    In cormack lehan classification of laryngoscopy view

    30 min after ultrasound measurements at time of induction of anesthesai

Secondary Outcomes (12)

  • Hyomental distance in neutral position

    30 min before operation

  • Throhyoid distance in neutral position

    30 min before operation

  • Cricothyriod distance in neutral position

    30 min before operation

  • Anterior soft tissue thickness at level of hyoid bone in neutral position

    30 min before opeqrtio

  • Anterior soft tissue thickness at level of epiglottis in neutral position

    30 min befor operation

  • +7 more secondary outcomes

Other Outcomes (1)

  • Age

    30 min before operation

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

all population undergoining surgical operation requiring general anesthesia and endotracheal intubation

You may qualify if:

  • Adult patients above18 years old
  • Both sex
  • Requiring general anesthesia with endotracheal intubation

You may not qualify if:

  • Emergency surgery,
  • patients with limited mouth, head or neck movement,
  • patients with temporomandibular joint impairment,
  • fracture or tumors of mandible,
  • patients requiring awake intubation,
  • uncooperative patients,
  • any cervical spine limitation movement
  • neck swelling or tumor
  • Prominent teeth deformities.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo University

Cairo, Cairo Governorate, 12613, Egypt

Location

Related Publications (3)

  • Parameswari A, Govind M, Vakamudi M. Correlation between preoperative ultrasonographic airway assessment and laryngoscopic view in adult patients: A prospective study. J Anaesthesiol Clin Pharmacol. 2017 Jul-Sep;33(3):353-358. doi: 10.4103/joacp.JOACP_166_17.

  • Roth D, Pace NL, Lee A, Hovhannisyan K, Warenits AM, Arrich J, Herkner H. Airway physical examination tests for detection of difficult airway management in apparently normal adult patients. Cochrane Database Syst Rev. 2018 May 15;5(5):CD008874. doi: 10.1002/14651858.CD008874.pub2.

  • Gomes SH, Simoes AM, Nunes AM, Pereira MV, Teoh WH, Costa PS, Kristensen MS, Teixeira PM, Pego JM. Useful Ultrasonographic Parameters to Predict Difficult Laryngoscopy and Difficult Tracheal Intubation-A Systematic Review and Meta-Analysis. Front Med (Lausanne). 2021 May 28;8:671658. doi: 10.3389/fmed.2021.671658. eCollection 2021.

Study Officials

  • ayman ali ghoneim, MD in anesthesia

    national cancer institute in egypt

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 11, 2024

First Posted

November 21, 2024

Study Start

March 20, 2023

Primary Completion

March 1, 2026

Study Completion

March 1, 2026

Last Updated

April 28, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will share
Shared Documents
STUDY PROTOCOL
Time Frame
for 1 year

Locations