Combined Ultrasound and Upper Lip Bite Test Assessment of Difficult Laryngoscopy in Obese Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorCairo University

About this trial

The aim of this observational study is to evaluate the accuracy of the HMDR combined with the ULBT as a predictor of difficult laryngoscopy in obese patients undergoing elective surgery under general anesthesia, regarding:

* Correlation of HMDR-ULBT values with Cormack-Lehane grades during laryngoscopy. * Comparison of HMDR-ULBT with standard HMDR in predicting difficult laryngoscopy.

Eligibility criteria

Qualifiers

Adult obese patients aged 18 to 65 years.

Both sexes.

American Society of Anesthesiologists (ASA) physical status II- III.

Body Mass Index (BMI) ≥ 30 kg/m² (classified as obese).

Disqualifiers

History of maxillofacial trauma, surgery, or congenital facial anomalies affecting mandibular movement or neck anatomy.

Known or suspected difficult airway requiring awake intubation.

Patients with limited neck mobility (e.g., cervical spine disease or immobilization).

Temporomandibular joint disorders or restricted mandibular mobility.

Trial design

Treatments tested in this trial

  • Hyomental distance measured using ultrasound in neutral head position, maximum head extension and during upper lip bite test

Treatment groups

134 Participants
are divided into 1 treatment group

Sponsors and collaborators