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

This trial does not accept healthy volunteers

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

Design model

Single group

Treatments tested in this trial

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

    Diagnostic test

    Hyomental distance will be measured using ultrasound in three positions: neutral head position, maximum head extension, and during the upper lip bite test (ULBT).

Treatment groups

134 Participants
are divided into 1 treatment group
Group A: HMD measured by US in neutral head position , maximum head extension and during upper lip bite testOther 1 intervention

Trial outcomes

Primary outcomes

1

Prediction of difficult laryngoscopic view, defined as Cormack-Lehane Grade 3 or 4 on the first laryngoscopy attempt without external laryngeal manipulation.

Difficult laryngoscopic view is defined as Cormack-Lehane Grade III or IV during the first laryngoscopy attempt without external laryngeal manipulation Cormack-Lehane classification for laryngoscopic view : grade 1: most of the vocal cords is seen; grade 2: only the posterior part of the vocal cords or the arytenoid cartilages are seen; grade 3: only epiglottis is seen; grade 4: epiglottis is not seen.

Time frame
Day of surgery from preoperative assessment to first laryngoscopy attempt after induction of general anethesia and after three minutes of mask ventilation.

Secondary outcomes

1

Determination of an optimal cutoff value for HMDR-ULBT to predict difficult laryngoscopy.

Receiver operating characteristic (ROC) curve analysis will be performed to determine the optimal cutoff value of the hyomental distance ratio measured during the upper lip bite test (HMDR-ULBT) for predicting difficult laryngoscopic view, defined as Cormack-Lehane Grade III or IV on the first laryngoscopy attempt without external laryngeal manipulation. The area under the ROC curve (AUC), sensitivity, specificity, positive predictive value, and negative predictive value corresponding to the optimal cutoff value will be calculated.

Time frame
From preoperative airway assessment until completion of the first laryngoscopy attempt during induction of anesthesia on the day of surgery
2

Comparison of HMDR-ULBT with standard HMDR in predicting difficult laryngoscopy.

The predictive performance of the hyomental distance ratio measured during the upper lip bite test (HMDR-ULBT) will be compared with that of the standard hyomental distance ratio (HMDR) for predicting difficult laryngoscopic view, defined as Cormack-Lehane Grade III or IV during the first laryngoscopy attempt without external laryngeal manipulation. Diagnostic accuracy parameters, including sensitivity, specificity, positive predictive value, negative predictive value, and area under the receiver operating characteristic (ROC) curve, will be compared between the two methods.

Time frame
From preoperative airway assessment until completion of the first laryngoscopy attempt during induction of anesthesia.

Other outcomes

Sponsors and contacts

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