Vancomycin Clinical Trial
Official title:
The Influencing Factors of Vancomycin Trough Level and the Rate Achieving the Target Trough Level in Critically Ill Patients: A Retrospective Observational Study
Verified date | January 2019 |
Source | Southeast University, China |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this study was to assess factors that may influence vancomycin trough level and the rate achieving the target trough level in critically ill patients.
Status | Completed |
Enrollment | 165 |
Est. completion date | December 31, 2017 |
Est. primary completion date | December 31, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Adult ICU patients (age=18 years) treated with intravenous vancomycin were included Exclusion Criteria: - Chronic renal dysfunction and acute renal injury patients treated with Renal Replacement therapy - VTL was not retained at steady-state - Vancomycin treatment time=48h - Vancomycin dose did not meet study definitions - Palliative care |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Southeast University, China |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of patients achieving the target vancomycin trough(15-20mg/L) | Vancomycin trough level was retained at steady state (after the third dose). If a patient has multiple measurements of vancomycin trough level, the first measurement is collected.Rate of patients achieving the target trough level (15-20mg/L) was observed. | 3 years |
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