Bassett Medical Center
Cooperstown, New York, 13326, United States
NCT Number: NCT07556107
The VPT Safety Trial (VPS) compares two common antibiotic combinations to see how they affect the kidneys of patients in the hospital with serious infections. Both combinations are approved by the Food and Drug Administration (FDA). The goal is to help doctors know which combination is safer so they can make better choices for their patients.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 4
Cooperstown, New York, 13326, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
PT Dosing (concealed): PT dosing is standard irrespective of infection severity.
4.5 gm IV loading dose over 30 min, then 4.5 g IV over 4 hr (extended infusion) 6 hrs after the loading dose, and then q 8 hr
M dosing (concealed): M dosing depends on infection severity.
1 gm loading IV dose over 30 min, then 1 gm IV over 4 hr (extended infusion) q 8 hr (default dosing).
Clinician has option to increase to 2 gm IV q 8 hr for severe infections and to decrease back to default dosing if previously chosen higher dosing is no longer deemed indicated.
Time frame: 7 days
Difference between highest Scys (mg/L) post-treatment over 7 days minus Scys pre-treatment, expressed as ratio of pre-treatment level
Time frame: 7 days
AKI/death KDIGO ADQI stages 0-4 (expanded with injury biomarkers) (Scr-Scys, Scys, Scr based) (transient <72 vs. persistent >72 hr) rate
Time frame: 90 days
MDR (MRSA, VRE, ESBL, CRE)/fungal/CDI rate
Time frame: 7 days
Difference between highest Scr (mg/L) post-treatment over 7 D minus Scr pre-treatment, expressed as ratio of pre-treatment level
Time frame: 90 days
NGAL, TIMP-2×IGFBP7, KIM-1, ACR
Contact information is provided by the study sponsor or research team.
Amanda Hasuly
CONTACT
Jennifer Victory
CONTACT
Bassett Healthcare
Other
A Randomized Controlled Trial Comparing Renal Effects of Vancomycin Combined With Either Piperacillin/Tazobactam or Meropenem: VPT Patient Safety (VPS) Study
Acronym: VPS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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