The use of gastric content to predict poor outcomes in medical critically ill patients
- Conditions
- gastric contentcritical illnessgastric pHpoor prognosisoutcomesproteomicsmetabolomicsgastric contentcritical illnessgastric pHpoor prognosisoutcomesproteomicsmetabolomics
- Registration Number
- TCTR20220530004
- Lead Sponsor
- The Faculty of Medicine Research Fund
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- nknown
- Sex
- All
- Target Recruitment
- 79
Inclusion Criteria
The patient who has nasogastric tube insertion on the first day of ICU admission.
Exclusion Criteria
The exclusion criteria are the patients who previously received PPIs or anti-histamine-2 receptor (H2RAS), unable to insert an NG tube on the first date, have upper GI bleeding, are pregnant, and refuse to participate in the study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Composite outcomes of death, CDI, VAP, and SRMD 28 days proportion
- Secondary Outcome Measures
Name Time Method n/a n/a n/a