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

Withdrawn

• Conditions: General Surgery
• Interventions: Other: Ultrasound

• Registration Number: NCT02940236
• Lead Sponsor: Mayo Clinic

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2016-10
• Study First Submitted: 2016-10-19
• Study First Submitted QC: 2016-10-19
• Study First Posted: 2016-10-20
• Primary Completion: 2018-02
• Study Completion: 2018-02
• Status Verified: 2023-03
• Last Update Submitted: 2023-03-22
• Last Update Posted: 2023-03-24

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

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

Exclusion Criteria

• BMI > 40

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Multimodal analgesia	Ultrasound	Patients scheduled for general surgery and requiring multimodal analgesia in preoperative period.

Primary Outcome Measures

Name	Time	Method
Oral multimodal analgesia and gastric volume	Baseline

Trial Locations

Locations (1)

Mayo Clinic Florida; 🇺🇸 Jacksonville, Florida, United States