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Ultrasound Assessment of Gastric Content for Semi Emergency Surgery

Ultrasound Assessment of Gastric Content for Semi Emergency Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02386787
Acronym
ECHO-GAST
Enrollment
300
Registered
2015-03-12
Start date
2014-05-31
Completion date
2016-04-30
Last updated
2016-05-25

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

Conditions

Anesthesia, Surgical Procedure, Unspecified

Keywords

Ultrasonography, Non-elective surgery, Anesthesia

Brief summary

Aspiration of gastric content is a rare but serious complication of anesthesia. In this context, preoperative fasting for elective surgery is well defined. In an emergency situation, international guidelines recommend rapid sequence of anesthesia to reduce the risk of aspiration. In semi emergency situation, there is no consensus about the anesthetic procedure even if a preoperative fasting has been observed due to uncertainty of gastric emptying related to stress or painful condition. The choice of anesthesia induction technique depends mainly on the anesthetist. Ultrasonography is a non invasive bedside tool that can provide reliable quantitative information about the volume of gastric content.

Interventions

DEVICEUltrasonography

an ultrasonography will be conducted before the anesthesic procedure to provide reliable quantitative information about the volume of gastric content.

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* undergoing a non-elective surgery * having a preoperative fasting period of six hours

Exclusion criteria

* patients with digestive diseases (gastroesophageal reflux disease, hiatal hernia, active peptic ulcer, upper gastrointestinal bleeding, vagal denervation, pyloric stenosis, extrinsic digestive compression, occlusive syndrome), neurologic diseases (spinal cord injury over T10, amylose, Shy-Drager syndrome) * patients with full stomach (preoperative fasting under 6 hours), * pregnant women (over 15 weeks of amenorrhea) * patients who received premedication.

Design outcomes

Primary

MeasureTime frameDescription
patients with full stomachbaselineFull stomach is defined by an antral cross-section area (CSA) \> 410 mm2, measured by ultrasonography

Secondary

MeasureTime frameDescription
preoperative painbaselineVisual Analog Scale
feeling of hungerbaseline
duration of preoperative fastingbaseline
type of surgery diseasebaseline
type of anesthetic procedure performedbaselinerapid or standard anesthetic induction
inhalation of gastric contentsbaselinenumber of patients with inhalation of gastric contents during intervention
nausea and vomitingbaselinenumber of patients with nausea and vomiting

Countries

France

Outcome results

None listed

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