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NCT02940236 Clinical Trial

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

General Surgery Clinical Trial

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

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02940236
Other study ID # 16-002313
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date October 2016
Est. completion date February 2018

Study information
Verified date March 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date February 2018
Est. primary completion date February 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients able to take prescribed oral multimodal analgesia as per standard of care Exclusion Criteria: - BMI > 40

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Ultrasound
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).

Locations
Country Name City State
United States Mayo Clinic Florida Jacksonville Florida

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Oral multimodal analgesia and gastric volume Baseline
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