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Ultrasound-Guided Breathing Pressure During Mask Ventilation in Obese Patients

Tests ultrasound-guided breathing pressure during mask ventilation in adults with severe obesity.

Plain-language title generated from the registry record
Registry title: Determination of the Optimal Inspiratory Pressure to Decrease Incidence of Gastric Insufflation With Adequate Ventilation During Facemask Ventilation in Morbidly Obese Patients

Key facts

Where
Banhā, EgyptSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07480031, who can take part

Where in Egypt

  • Benha University HospitalsBanhā, EgyptNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Benha University
Trial code
NCT07480031
Record updated
18 March 2026
Original description
The goal of this randomized clinical trial is to optimize the inspiratory pressure during facemask ventilation (FMV) in morbidly obese patients (BMI ≥40 kg/m²), to ensure adequate ventilation while minimizing the risk of gastric insufflation by real-time ultrasound guidanceRead full original descriptionShow less

Ultrasound-Guided Optimization of Inspiratory Pressure During Facemask Ventilation in Morbidly Obese Patients to Prevent Gastric Insufflation: A Randomized Clinical Trial

The goal of this randomized clinical trial is to optimize the inspiratory pressure during facemask ventilation (FMV) in morbidly obese patients (BMI ≥40 kg/m²), to ensure adequate ventilation while minimizing the risk of gastric insufflation by real-time ultrasound guidance

Inclusion: Adult patients (18-65 years old) scheduled for elective surgery under general anesthesia requiring facemask ventilation; Morbid obesity (BMI ≥40 kg/m²); American Society of Anesthesiologists (ASA) physical status II-III; Normal upper gastrointestinal anatomy (no history of gastric surgery, esophageal strictures, or hiatus hernia); Fasted for at least 6 hours for solids and 2 hours for fluids (standard preoperative fasting guidelines).

Exclusion: • Emergency surgery (due to inability to ensure proper fasting or preoperative assessment); Known or suspected difficult airway (Mallampati class IV, limited neck mobility, or history of difficult intubation); Gastroesophageal reflux disease (GERD) or high aspiration risk (e.g., pregnancy, symptomatic hiatal hernia); Contraindications to facemask ventilation (facial trauma, beard/mask seal interference); Severe cardiopulmonary disease (e.g., severe COPD, pulmonary hypertension, or unstable angina); Neuromuscular disorders affecting respiratory function; Refusal to participate or inability to provide informed consent.

ClinicalTrials.gov NCT07480031