Premedication Gastric Ultrasound

Part of paid clinical trials in Columbus, Ohio.

Sponsor
Kevin Spellman
Study ID
NCT04130022
Status
Enrolling By Invitation

Conditions

  • Surgery

Eligibility Criteria

Sex
ALL
Age
0 Years - 18 Years
Healthy Volunteers
Not accepted

Interventions

  • Point-of-Care Ultrasound — DEVICE
    Portable ultrasonography done at the bedside.

Study Details

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.

Key Dates

Start date
Aug 18, 2025
Status verified
Aug 2025
Primary completion
Dec 31, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
100 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC

Arms

  • Other: Fasted Children

Primary Outcome Measure

Change of Qualitative and Quantitative Gastric Assessment After Premedication [ Time Frame: Ultrasound scan performed at baseline (before surgery) to measure gastric volume and 3 minutes after taking premedication to assess change. ]

Locations (1)

FacilityCityStateZIPSite coordinators
Nationwide Children's HospitalColumbusOhio43205-

Find similar trials in Columbus, OH

By research site
Nationwide Children's Hospital· Columbus, OH

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