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Blind Gastric Tube Placement: Incidence of Malposition Confirmed by Ultrasonography

Completed
Conditions
Anesthesia
Interventions
Other: Blind Gastric Tube Placement
Registration Number
NCT03430908
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Brief Summary

This is a prospective, single-arm cohort, observational study to determine the incidence of gastric tube malposition during blind insertion by an anesthesia provider.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
166
Inclusion Criteria
  • The adult population, ages 18 and greater
  • Patients undergoing general anesthesia with an endotracheal tube that will have a gastric tube blindly inserted by an anesthesia provider
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Exclusion Criteria
  • Pediatric population (<18 years)
  • Gastric tube inserted under direct visualizing (the use of a Mac or Miller laryngoscope or any video laryngoscope)
  • Inability to visualize gastric tube by ultrasound due to body habitus, analogous anatomy, etc
  • Pre-anesthesia insitu gastric tube
  • Gastric tube inserted by practitioner other than a member of the anesthesia team
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Participants with an endotracheal tubeBlind Gastric Tube PlacementParticipants undergoing general anesthesia with an endotracheal tube will have a gastric tube blindly inserted by an anesthesia provider.
Primary Outcome Measures
NameTimeMethod
Incidence of malposition of blindly placed gastric tubes by anesthesia providersDay of procedure
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Memorial Sloan - Kettering Cancer Center

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New York, New York, United States

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