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

NCT ID: NCT02940236

Last Updated: 2023-03-24

Basic Information

• Recruitment Status: WITHDRAWN
• Study Classification: OBSERVATIONAL
• Study Start Date: 2016-10-31
• Study Completion Date: 2018-02-28

Brief Summary

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

Conditions

General Surgery

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Study Groups

Multimodal analgesia

Patients scheduled for general surgery and requiring multimodal analgesia in preoperative period.

Ultrasound

Intervention Type: OTHER

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).

Interventions

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).

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

• BMI > 40

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Mayo Clinic

OTHER

Sponsor Role: lead

Responsible Party

Elird Bojaxhi, M.D.

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Mayo Clinic Florida

Jacksonville, Florida, United States

Countries

United States

Other Identifiers

16-002313

Identifier Type: -

Identifier Source: org_study_id