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Premedication Gastric Ultrasound

K

Kevin Spellman

Status

Invitation-only

Conditions

Surgery

Treatments

Device: Point-of-Care Ultrasound

Study type

Interventional

Funder types

Other

Identifiers

NCT04130022
STUDY00000586

Details and patient eligibility

About

The primary objective of this study is to assess gastric volume in fasted children using ultrasound before and after drinking premedication. The hypothesis is that the qualitative and quantitative assessment by gastric ultrasound in the stomach before and after drinking premedication will be the same as premedication has a small volume.

Enrollment

100 estimated patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA 1-2 patients aged 0-18 years of scheduled for elective surgery under general anesthesia.

Exclusion criteria

  • Patients who are not adhere to institutional fasting guidelines.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Fasted Children
Other group
Treatment:
Device: Point-of-Care Ultrasound

Trial contacts and locations

1

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Central trial contact

Julie Rice-Weimer; Catherine Roth

Data sourced from clinicaltrials.gov

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