Gastric Volumes After Oral Multimodal Analgesia in the Pre-operative Setting: A Prospective Case Series

Gastric Volumes After Oral Multimodal Analgesia in the Pre-operative Setting

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02940236

Enrollment

Registered

2016-10-20

Start date

2016-10-31

Completion date

2018-02-28

Last updated

2023-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

General Surgery

Brief summary

To assess possible risk of aspiration with pre-operative oral medications taken with sips of water (100ml).

Interventions

OTHERUltrasound

Before and after patient receives oral multimodal analgesia as per standard of care, two ultrasound scans will be performed (10 minutes apart for each time element).

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Patients able to take prescribed oral multimodal analgesia as per standard of care

Exclusion criteria

* BMI \> 40

Design outcomes

Primary

Measure	Time frame
Oral multimodal analgesia and gastric volume	Baseline

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026