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Gastric US in ICU Patient

Gastric Ultrasound in Critically Ill Patients for Evaluation of Gastric Volume Residuals; A Comparison of NPO Protocols

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05526105
Enrollment
50
Registered
2022-09-02
Start date
2023-02-03
Completion date
2025-02-03
Last updated
2024-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aspiration Pneumonia, Critical Illness, Surgery

Keywords

NPO Protocols, Intensive Care Unit, Gastric Ultrasound, Ultrasound, Surgical Intensive Care Unit, NPO, Nasogastric Tube, Orogastric Tube, Enteral Nutrition, Parenteral Nutrition, Gastric Residual Volume, Aspiration, Critical Illness Nutrition

Brief summary

This is a case series study using gastric ultrasound in critically ill patients to quantify gastric residual volumes to compare the efficacy of different NPO protocols.

Interventions

DIAGNOSTIC_TESTGastric Ultrasound

Gastric ultrasound in the supine and right lateral decubitus position for patients going for operative intervention with a protected airway.

Sponsors

Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Intervention model description

Patients will be assigned to be NPO after midnight (standard protocol) or feed up until call to OR then decompressed (liberal protocol).

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Patients age 18 or older, admitted to the ICU, requiring general anesthesia or sedation for a procedure with a pre-existing, cuffed endotracheal or tracheostomy tube. Most patients admitted to the ICU would be unable to consent.

Exclusion criteria

* Known upper gastrointestinal anatomical problem that would prevent accurate estimation of gastric volume, gastric perforation, pregnancy beyond the first trimester. * Lack of a pre-existing, cuffed endotracheal or tracheostomy tube.

Design outcomes

Primary

MeasureTime frameDescription
Gastric Residual VolumesWithin one hour of operative intervention.Quantification of gastric residual volumes as measured in milliliters using antral cross-sectional areas and semi-quantitative gastric volumes using standardized grading scores.

Secondary

MeasureTime frameDescription
Comparison of two different NPO protocol populationsWithin four months of study completion, 16 months from study startComparing standard ASA NPO protocol vs liberal, feed-up-until-call to OR protocol as defined by comparison of gastric volumes (mLs).
Peri-operative aspiration eventsWithin four months of study completion, 16 months from study startNumber of aspiration events per number of operative interventions.
Estimation of the amount of enteral nutrition lost prior to surgery using the different NPO protocolsZero to sixteen hours prior to surgeryCalculation of enteral nutrition held during NPO time in kilocalories.

Countries

United States

Contacts

Primary ContactLaura M Chiang, MD
laura.m.chiang@hitchcock.org6036500360
Backup ContactLaura M Chiang, MD
laura.m.chiang@hitchcock.org6036505922

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026