beta
Trial Radar AI
Clinical Trial NCT07493356 for Ventilatory Defect, Intubation; Difficult or Failed is recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here.
One study matched filter criteria
Card View

Difficult Airway Prediction by Integrating STOP-BANG Criteria 233

Recruiting
Clinical Trial NCT07493356 is an observational study for Ventilatory Defect, Intubation; Difficult or Failed that is recruiting. It started on 9 March 2026 with plans to enroll 233 participants. Led by Sindh Institute of Urology and Transplantation, it is expected to complete by 8 September 2026. The latest data from ClinicalTrials.gov was last updated on 25 March 2026.
Brief Summary
This study is being done to determine the diagnostic accuracy of the STOP-BANG questionnaire in predicting difficult mask ventilation and intubation among obese patients.

During the preoperative assessment, eligible participants will be enrolled in the study. The modified Mallampati score, thyromental distance, mouth opening, and upper lip bite tests will be performed along with STOP-Bang scores.

Later in the opera...

Show More
Detailed Description
After approval of the Ethical Review Committee (ERC), the study will commence. Participants will be selected from the scheduled elective surgical lists of all surgical departments. Written informed consent will be acquired from all study participants. The resident will document demographic variables (age, height, weight, and gender) and STOP-Bang scores during the pre-anesthesia assessment for eligible participants. ...Show More
Official Title

Enhancing Difficult Airway Prediction in Obese Patients: Integrating STOP-BANG With Additional Airway Assessment Tools

Conditions
Ventilatory DefectIntubation; Difficult or Failed
Other Study IDs
  • SIUT-ERC-2025/A-587
NCT ID Number
Start Date (Actual)
2026-03-09
Last Update Posted
2026-03-25
Completion Date (Estimated)
2026-09-08
Enrollment (Estimated)
233
Study Type
Observational
Status
Recruiting
Keywords
Laryngoscopy
Ventilation of lungs
Bag-mask
General Anesthesia
Primary Outcome Measures
Outcome MeasureMeasure DescriptionTime Frame
Adequate Bag-Mask Ventilation
When an anesthetized patient is being manually ventilated by an anesthesia bag and a face mask and achieving a tidal volume of 5 ml/kg, it will be called adequate mask ventilation. * Easy if a single anesthesiologist achieves visible adequate chest rise and an end-tidal CO₂ graph. * Moderately difficult, if there is a slight chest rise, a low end-tidal CO₂ graph, but peripheral oxygen saturation is maintained above 97%. * Difficult if there is no visible chest rise, minimal or no end-tidal CO₂ graph, or if peripheral oxygen saturation drops to less than 95% but becomes normal with use of an oral airway (Guedel airway) or a laryngeal mask airway (LMA), or if two anesthesia providers are required for adequate mask ventilation. * Very difficult if peripheral oxygen saturation drops to 90% or less despite the use of airway adjuncts (Guedel airway or LMA).
Only once, after giving general anesthesia but before an endotracheal tube is put in the trachea
Difficult Tracheal Intubation
Difficult tracheal intubation will be defined as, one that requires external laryngeal manipulation, laryngoscopy requiring more than 3 attempts at intubation, intubation requiring nonstandard equipment or approaches, or the inability to intubate at all
Only once, after giving general anesthesia and 3-minute bag-mask ventilation for adequate muscle relaxation effect, then direct laryngoscopy will be performed to put the endotracheal tube in the trachea
Participation Assistant
Eligibility Criteria

Eligible Ages
Adult
Minimum Age
18 Years
Eligible Sexes
All
  • Male & Female aged 18-60 years.
  • Body mass index 30 or more
  • American Society of Anesthesiologists (ASA) status II-III.
  • Scheduled for elective surgery under general anesthesia with endotracheal intubation.

  • Patients' refusal to participate.
  • American Society of Anesthesiologists (ASA) IV & V.
  • Neuromuscular diseases or facial abnormalities.
  • Cardiothoracic, head and neck, or emergency surgery.
  • Previously diagnosed with OSA (by polysomnography) will be excluded.
  • Any airway-related anatomical deformity (e.g., Down's syndrome).
  • History of radiation exposure.
  • Patient with mouth opening <2 fingers
Sindh Institute of Urology and Transplantation logoSindh Institute of Urology and Transplantation
Study Responsible Party
Syed Muhammad Abbas, Principal Investigator, Professor, Sindh Institute of Urology and Transplantation
Study Central Contact
Contact: Syed M Abbas, FCPS, 02199215718, [email protected]
1 Study Locations in 1 Countries

Sindh

Sindh Institute of Urology and Transplantation, Karachi, Sindh, 74200, Pakistan
Syed M Abbas, FCPS, Contact, +923331318838, [email protected]
Recruiting