Skip to content

Vancomycin-Associated Acute Kidney Injury: A Cross-Sectional Study From a Multi- Center in China

Vancomycin-Associated Acute Kidney Injury: A Cross-Sectional Study From a Multi- Center in China

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03456544
Enrollment
10000
Registered
2018-03-07
Start date
2018-10-31
Completion date
2019-12-31
Last updated
2019-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury, Adverse Effect, Cross-sectional Study, Staphylococcal Infections, Vancomycin

Brief summary

The objective of this study was to investigate the current situation of vancomycin (VAN)-associated acute kidney injury (VA-AKI) in China and identify the risk factors for VA-AKI, as well as to comprehensively examine the risk related to concurrent drug use. Further, the investigators assessed the outcomes of patients who developed VA-AKI and the risk factors for these outcomes. Finally, the investigators aimed to provide suggestions for improving the prevention and treatment of VA-AKI in China.

Interventions

DRUGVancomycin

Patients who have vancomycin associated acute kidney injury will be in the Van-AKI group, and those who don't have vancomycin associated acute kidney injury will be in the none VAN-AKI group.

Sponsors

Peking University First Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Using Vancomycin * ≥18 years old

Exclusion criteria

* Medical records were incomplete * Had been diagnosed with stage 5 CKD or were regularly receiving dialysis * SCr were not being adequately monitored to detect the development of AKI * Had undergone nephrectomy

Design outcomes

Primary

MeasureTime frame
Vancomycin-associated acute kidney injury(VAN-AKI) occuration rate1 year

Secondary

MeasureTime frame
VAN-AKI detection rate1 year
TDM detction rate1 year
0h Serum creatinine detction rate1 year
48h Serum creatinine detction rate1 year

Countries

China

Contacts

Primary ContactLingyun Ma
haily618@163.com008601066110802

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026