Gastric Volumes After Oral Multimodal Analgesia in the Pre-operative Setting: A Prospective Case Series
Withdrawn
- Conditions
- General Surgery
- 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
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- WITHDRAWN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
- Primary Outcome Measures
Name Time Method Oral multimodal analgesia and gastric volume Baseline
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms link oral multimodal analgesia to gastric volume changes pre-operatively in NCT02940236?
How does pre-operative oral analgesia with sips of water compare to standard NPO protocols in reducing aspiration risk for general surgery patients?
Which biomarkers correlate with gastric volume retention after multimodal analgesia in the pre-operative setting (NCT02940236)?
What adverse events are associated with ultrasound-measured gastric volumes in patients receiving pre-operative oral analgesia?
Are combination analgesia regimens (e.g., NSAIDs + acetaminophen) more effective than single-agent approaches in managing gastric emptying pre-surgery?
Trial Locations
- Locations (1)
Mayo Clinic Florida
🇺🇸Jacksonville, Florida, United States
Mayo Clinic Florida🇺🇸Jacksonville, Florida, United States