Clinical Trials Directory

Trials / Completed

CompletedNCT04088305

Vancomycin Dosage Strategy Based on a Trough Concentration Model

Clinical Evaluation of a Vancomycin Dosage Strategy Based on a Serum Trough Concentration Model in Elderly Patients With Severe Pneumonia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Peking University Third Hospital · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

Study design: Allocation: Randomized Endpoint classification: Efficacy study Masking: Open label Primary purpose: Treatment Primary endpoint: Incidence of reaching the target serum trough concentration Secondary endpoint: Clinical efficiency, Antibiotic use, acute kidney injury.

Detailed description

This is a prospective randomized control trial. There are two groups, study group and control group. Patients of study group accepted vancomycin strategies decided by a serum trough concentration model, and patients of control group accepted vancomycin dosage decided by attending physician. The primary endpoint is the incidence of reaching the target serum trough concentration, the secondary endpoint are clinical efficiency, antibiotic use and side effects such as acute kidney injury, etc.

Conditions

Interventions

TypeNameDescription
DRUGIndividualized therapyDosage of Vancomycin decided by a serum trough concentration model, instead of decided by attending physician

Timeline

Start date
2019-10-01
Primary completion
2022-05-31
Completion
2022-06-30
First posted
2019-09-12
Last updated
2022-08-31

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04088305. Inclusion in this directory is not an endorsement.