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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03205774
Other study ID # L16-190
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 3, 2017
Est. completion date January 20, 2018

Study information

Verified date May 2018
Source Hôpital Edouard Herriot
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this prospective study was to assess the effect of patient positioning on the ultrasound assessment of gastric contents.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date January 20, 2018
Est. primary completion date January 20, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ASA 1 and 2 volunteers

Exclusion Criteria:

- Diabetes mellitus

- previous gastrointestinal surgery

- Medication affecting gastric motility

- digestive diseases, gastroparesis

- Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
6 hours fasting and free oral intake of water
Ultrasound examination of the gastric antrum are performed in volunteers after prolonged fasting and 10 min after oral intake of water. Volunteer should be lying on his/her back, right lateral decubitus position and left lateral decubitus position with randomization of the order.

Locations

Country Name City State
France Hôpital Femme Mère Enfant Lyon

Sponsors (1)

Lead Sponsor Collaborator
Hôpital Edouard Herriot

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in ultrasound measurement of the antral cross sectional area according to the position Ultrasound measurement of antral cross-sectional area through study completion, an average of 20 min
Primary Change in qualitative ultrasound assessment of gastric contents according to the position qualitative ultrasound assessment of gastric contents through study completion, an average of 20 min
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