Ultrasound Assessment of Gastric Content in Fasted Pregnant Women

  • STATUS
    Recruiting
  • participants needed
    1200
  • sponsor
    University Hospital, Montpellier
Send
Updated on 16 February 2024
See if I qualify

Summary

Pulmonary aspiration of gastric content is one of the most feared perioperative complication of general anesthesia. Pregnant women are usually considered as high risk of pulmonary aspiration but there is no epidemiological study evaluating gastric content in pregnant women during the entire gestation periode.

The main objective is evaluating prevalency of "full stomach" in differents stages of pregnancy in fasted pregnant women.

Description

Subjects will be recruited at Montpellier University Hospital, from fasted pregnant women before surgery or from ultrasound exam performed during pregnancy.

Details
Condition Fasting, Pregnant woman, Gastric Ultrasound
Age 18years - 100years
Clinical Study IdentifierNCT04277013
SponsorUniversity Hospital, Montpellier
Last Modified on16 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

An subject must fulfill all of the following criteria in order to be eligible
for study
enrollment
Aged at least 18 years old
Pregnant women
Fasted ( at least 6h for solid , 2h for clear fluid )

Exclusion Criteria

Previous Bariatric surgery / upper gastro-intestinal surgery
Adult under protection
Clear my responses
Read more

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.