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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02819466
Other study ID # PI2012_843_0027
Secondary ID
Status Completed
Phase N/A
First received June 28, 2016
Last updated June 28, 2016
Start date April 2013
Est. completion date June 2015

Study information

Verified date June 2016
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Observational

Clinical Trial Summary

Aspiration pneumonia is a dreaded complication of anaesthesia because of its prevalence (1/3,886 cases in elective anaesthesia and 1/895 cases in emergency settings) and its high morbidity and mortality (3 to 9%). This chemical and/or infectious pneumonia is secondary to passage of the gastric contents into the unprotected upper airways during general anaesthesia. The prognosis depends on three factors: the presence of food debris, and the acidity and volume of the gastric contents. To prevent this complication, the French society of anaesthesia and intensive care recommends preoperative fasting rules and, in patients presenting risk factors for aspiration, the use of antacids and rapid sequence intubation. This preventive strategy is associated with certain adverse events: deferred operative procedures, discomfort and hypoglycaemia secondary to fasting, more frequent anaphylactic complications, and memory of anaesthetic induction.

Over recent years, ultrasound has become more widely used by anaesthetists for local anaesthesia, vascular catheterization, haemodynamic monitoring and, more recently, 2D ultrasound estimation of intragastric volume. However, 2D ultrasound estimation of intragastric volume presents several limitations: because of the complex shape of the stomach, this technique requires a long learning curve and the measured volume is poorly correlated with reference techniques (MRI and 99Tc scintigraphy). Two studies have recently measured intragastric volume by three dimensional ultrasound with promising results.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Healthy volunteers over the age of 18 years employed by Amiens University Hospital and covered by French national health insurance.

- Fasting (last meal > 6 hours and last drink of water, tea or coffee > 2 hours)

- Signature of the free and informed written consent form.

Exclusion Criteria:

- Pregnant woman.

- Presence of diseases or treatments that alter (slow or accelerate) gastric emptying.

- Presence of swallowing disorders.

- History of gastric or supramesocolic surgery.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Echocardiography, Three-Dimensional

Intervention

Device:
3D echography
ultrasound visualization of the stomach in fasting patients.

Locations

Country Name City State
France CHU Amiens Amiens

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary success rate of ultrasound visualization of the stomach while fasting success rate of ultrasound visualization of the stomach while fasting Day 0 No
Secondary ultrasound visualization of the fasting stomach learning curve ultrasound visualization of the fasting stomach learning curve for each investigator Day 0 No
Secondary measured difference of antral surface area antral surface area after ingestion of fluid - fasting antral surface area Day 0 No
Secondary absolute error of the volume measured ingested volume - intragastric volume variation Day 0 No
Secondary relative error of the volume measured (absolute error / ingested volume) * 100 Day 0 No
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