A prospective observational study of changes in blood levels of thiamine, ascorbic acid, cortisol, and copeptin in patients with sepsis
Not Applicable
Recruiting
- Conditions
- sepsis
- Registration Number
- JPRN-UMIN000044490
- Lead Sponsor
- Tohoku University Graduate School of Medicine Division of Emergency and Critical Care Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Not provided
Exclusion Criteria
Patients already diagnosed with sepsis at another hospital Patients who did not consent to this study Patients after cardiopulmonary arrest resuscitation Patients judged to be ineligible by attending physicians For patients who declined aggressive treatment by the third day of hospitalization, data after the decline of treatment will not be used.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 28-days mortality
- Secondary Outcome Measures
Name Time Method Changes in SOFA score on the 4th day Hospital mortality Refractory shock (inadequate hemodynamic response to noradrenalin administration)