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Preoperative Presence of Gastric Content in Non-fasting Patients - an Ultrasound Study

Completed
Conditions
Non-fasting Patients
Rapid Sequence Intubation
Anesthesia Intubation Complication
Interventions
Other: Bedside ultrasound
Registration Number
NCT03685435
Lead Sponsor
University Hospital, Akershus
Brief Summary

Using bedside ultrasound, the investigators will examine gastric content in non-fasting patients assigned to rapid sequence intubation (RSI). The procedure will be done immediately before intubation. The percentage of non-fasting patients who actually have gastric content will be determined.

Identifying gastric content is critical because presence increases the risk of pulmonary aspiration during intubation.

Detailed Description

Quantitative gastric content will be registered by measuring the cross section area of antrum using bedside ultrasound. The area and the patients age will be applied to estimate gastric volume.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
Inclusion Criteria
  • adults scheduled for surgery
  • Adults over 18 years old that are assigned to general anesthesia with rapid sequence intubation (RSI)
Exclusion Criteria
  • Body mass index over 40
  • Pregnant women
  • Patients earlier underwent gastric surgery
  • Critically ill patients where spending time on ultrasound would cause a major disadvantage for the patients

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Non-fasting patientsBedside ultrasoundWe will examine non-fasting patients using bedside ultrasound. First we examine the gaster in a supine position. Then we repeat the procedure in a right lateral position.
Primary Outcome Measures
NameTimeMethod
Low risk of aspirationImmediately before intubation

Detection of empty stomach, or less than 1,5 mL/kg clear fluid in the gaster

High risk of aspirationImmediately before intubation

Detection of solids, or more than 1,5 mL/kg clear fluid in the gaster

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Akershus University Hospital

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Lørenskog, Akershus, Norway

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