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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03806543
Other study ID # 2018ZDSYLL117-P01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2015
Est. completion date December 31, 2017

Study information

Verified date January 2019
Source Southeast University, China
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

This retrospective observational study included adult patients treated with intravenous vancomycin in intensive care unit of Zhongda Hospital from January 2015 to December 2017. Vancomycin dose was based on international consensus and adjusted according to estimated glomerular filtration rate (eGFR) calculated by the Cockcroft-Gault equation. vancomycin trough level (VTL) was retained at steady state (after the third dose). Linear regression was performed to determine the correlation between factors prior to the first vancomycin dose and VTL. Distribution of VTL and percentage of patients achieving the target trough level (15-20mg/L) was observed in different renal function.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Vancomycin
adult patients treated with intravenous vancomycin in intensive care unit

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Southeast University, China

Outcome

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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