CClinicalTrials.gg
RecruitingNCT06000267Updated Sep 13, 2023

Incidence and Contributing Anthropometric Factors of Difficult Airway in Pediatric Surgical Patients

An observational study in Difficult Airway, sponsored by University Childrens Hospital Belgrade. Recruiting at 1 site in Serbia. Open to participants aged 28 Days to 14 Years. Per ClinicalTrials.gov, last updated 2023-09-13.

Sponsored by University Childrens Hospital Belgrade · Observational

From the registry’s dates

  • Primary completion was expected by Oct 2023, 3 years ago, but the record still lists the study as recruiting.
  • Started Jan 2022; still recruiting 4 years 8 months later.
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
500
Ages
28 Days to 14 Years
Sex
All
01

Study summary

The goal of this prospective, observational study is to identify predictors of difficult mask ventilation, direct laryngoscopy and intubation in pediatric patients scheduled for elective surgery and to determine their incidence. As a final goal, the investigators will try to define new scoring system for difficult airway prediction. Participants will be pediatric patients age infant till school age. Participants will have their airway assessed one day before surgery by taking anthropometric measurements of face and neck. After iv anesthesia induction and application of muscle relaxant, the investigators will assess difficulty of face mask ventilation by using grading from 0-4. Direct laryngoscopy will be performed with Macintosh blade and experienced anesthesiologist will determine Cormack - Lehane score as well as intubation difficulty score (IDS).

Read the detailed description

Participants will be divided into groups: up to 1 yrs of age, 1-2.9 yrs, 3-4.9, 5-6.9, and 7 yrs and older.

The investigators will test predictive value, sensitivity and specificity of anthropometric parameters used for airway assessment in pediatric patients, as well as gender, age, BMI, ASA score.

Anatomical parameters that will be measured the day before surgery: chin, inter - incisor gap, hyomental distance (HMD), hyoid - thyroid distance (HT), neck circumference, neck length, neck extension, lower lip to chin distance (LCD), tragus to chin distance (TMA), thyromental distance (TMD), sternomental distance (SMD).

Mallampati test will be performed in children older than 5 years and best oropharyngeal view (BOV) will be determined for younger children. Colorado Pediatric Airway Score (COPUR) will be calculated.

All patients will be premedicated with midazolam 0.5 mg/kg orally, 30 minutes before intervention or 0.1 mg/kg iv. Anesthesia induction will be intravenous: thiopentone 5 mg/kg or propofol 2.5 mg/kg, fentanyl 3 mcg/kg and non depolarizing muscle relaxant rocuronium 1 mg/kg or cis-atracurium 0.15 mg/kg. Face mask ventilation will be quantified as grade 0-4. Anesthesia maintenance will be intravenous or inhalatory depending on anesthesiologists decision. Patients will be intubated with Macintosh blade in the supine position, without additional elevation of occipital part of the head. Difficult laryngoscopy is defined as CL grade III and IV and they predict difficult endotracheal intubation. Intubation difficulty score will be used to asses intubation. Intubation difficulty will be defined by IDS - intubation difficulty score > 5.

Standard procedures will be performed in case of difficult mask ventilation and intubation.

02

Conditions studied

  • Difficult Airway

Keywords

  • children
  • intubation
  • face mask ventilation
  • best oropharyngeal view
03

In context

Lead sponsor

This is the only study on the registry with University Childrens Hospital Belgrade as lead sponsor.

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

04

Who can participate

Ages eligible
28 Days to 14 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patient will be divided in 5 groups according to age: infants, children from 1 - 2,9 years, 3 - 4,9 years, 5 - 6,9 years and older than 7 years.

Inclusion criteria

  • Pediatric patients from one month to 14 years old scheduled for elective surgery in general endotracheal anesthesia.

Exclusion criteria

Exclusion Criteria:

  • Congenital syndromes which include difficult airway (Pierre Robin, Goldenhar syndrome, Treacher Collins syn, Down syn, Edwards, Arthrogryposis, Apart syn etc.), craniofacial dysmorphia, ENT, maxillofacial and cardiac surgery patients, patients with resent respiratory infections
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
500 participants (estimated)
Patient registry
No

Interventions

  • ProcedureIntubation

    All the patients will be ventilated with face mask and intubated before elective surgery

06

What researchers measure

Primary outcomes

  1. incidence of difficult mask ventilation and intubation

    Determination of grade 3 and 4 of mask ventilation incidence in different age groups of children and incidence of difficult intubation defined as intubation difficultly score \>5

    Time frame: one year

Secondary outcomes

  1. Identification of anthropometric parameters of face and neck which determine difficult airway in children

    Identification of preoperative measurements of face and neck determining difficult face mask ventilation and intubation

    Time frame: one year

07

Study locations

1 of 1 sites recruiting
  • University Children hospital
    Belgrade, 11000, Serbia
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 13, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06000267
Lead sponsor
University Childrens Hospital Belgrade
Responsible party
Ivana Petrov Bojicic (Associate Professor, University Childrens Hospital Belgrade) — Principal investigator
First posted
Aug 21, 2023
Start date
Jan 10, 2022
Primary completion
Oct 2023 (estimated)
Completion
Oct 2023 (estimated)
Last update
Sep 13, 2023

Study contacts

Ivana Petrov, MD
Contact
kikapetrov75@gmail.com
64 152 5959 ext. +381
Ivana Petrov, MD
principal investigator · University children hospital

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

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