The Influencing Factors of Vancomycin Trough Level and the Rate Achieving the Target Trough Level

NCT ID: NCT03806543

Last Updated: 2019-01-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

165 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-01-01

Study Completion Date

2017-12-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Vancomycin

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Interventions

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Vancomycin

adult patients treated with intravenous vancomycin in intensive care unit

Intervention Type DRUG

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Southeast University, China

OTHER

Sponsor Role lead

Responsible Party

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Jingyuan,Xu

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jingyuan Xu, PHD.

Role: PRINCIPAL_INVESTIGATOR

Southeast University

Other Identifiers

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2018ZDSYLL117-P01

Identifier Type: -

Identifier Source: org_study_id

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