Vancomycin in the Target Site Treatment of Intracranial Infection

NCT ID: NCT03585426

Last Updated: 2018-07-13

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

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-31

Study Completion Date

2018-12-31

Brief Summary

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Vancomycin, a novel intravenously administered antibiotic, currently plays a key role in the management of complicated multi-organism infections. However,current LC-MS/MS methods briefly describe parameters and the only reported internal standard was sometimes difficult to obtain. In our study,an updated LC-MS/MS method for the quantitative analysis of vancomycin in human serum was developed.

Detailed Description

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Conditions

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Vancomycin

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Vancomycin 1g q12h

Group Type EXPERIMENTAL

Vancomycin

Intervention Type DRUG

Vancomycin, a novel intravenously administered glycylcycline antibiotic, currently plays a key role in the management of complicated multi-organism infections.

Vancomycin 1g q8h

Group Type EXPERIMENTAL

Vancomycin

Intervention Type DRUG

Vancomycin, a novel intravenously administered glycylcycline antibiotic, currently plays a key role in the management of complicated multi-organism infections.

Interventions

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Vancomycin

Vancomycin, a novel intravenously administered glycylcycline antibiotic, currently plays a key role in the management of complicated multi-organism infections.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

In ICU; ventricle drainage was carried out; renal function is normal, namely creatinine clearance rate is \>60ml/min;

Exclusion Criteria

women in pregnancy or lactation;in patients with renal insufficiency, the creatinine clearance rate (Clcr) is less than 60ml/min.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Xijing Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Yanyan Jia, Dr.

Role: STUDY_DIRECTOR

The First Affiliated Hospital, the Fourth Military Medical University

Other Identifiers

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XJYY-LL-FJ-045

Identifier Type: -

Identifier Source: org_study_id

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