Actively Recruiting
Concentration of Unbound Cloxacillin in Adults Treated With Continuous Infusion Via Elastomeric Pump
Led by Emeli Månsson · Updated on 2026-02-17
25
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
E
Emeli Månsson
Lead Sponsor
R
Region Västmanland
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying adults with severe infections caused by the bacterium Staphylococcus aureus to understand how the antibiotic cloxacillin works when given continuously through an elastomeric pump. The study aims to measure the free (unbound) concentration of cloxacillin in the blood to ensure levels are appropriate—not too high or too low. This research will help develop a model to predict the best dosage for individuals based on factors like age, gender, kidney function, and protein levels in the blood. Participants will receive cloxacillin through a continuous infusion using an elastomeric pump. Blood samples will be collected before starting the infusion and then at 4 hours, 24 hours, and 48 hours after beginning the infusion. The study focuses on monitoring the unbound cloxacillin concentration at these time points to gather detailed information on how the drug behaves in the body during continuous treatment. During the study, participants will have blood drawn multiple times to measure cloxacillin levels and monitor their response. Researchers will use these measurements to develop a personalized dosing model. The main outcome tracked is the free cloxacillin concentration over the 48-hour infusion period. The study does not involve blinding or placebo control and is sponsored by Emeli Månsson. Participation lasts at least 48 hours from enrollment to the end of follow-up.
CONDITIONS
Brief Title
Unbound Cloxacillin Concentrations During Continuous Infusion
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Treating physician has decided to start continuous infusion of cloxacillin
You will not qualify if you...
- Unwilling or unable to provide written informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 48 hours
Participants receive continuous infusion of cloxacillin via an elastomeric pump.
Blood samples drawn before infusion, and after 4 hours, 24 hours, and 48 hours of continuous infusion
Trial Site Locations
Total: 1 location
1
Västmanlands sjukhus Västerås
Västerås, Sweden
Actively Recruiting
Research Team
E
Emeli Månsson, PhD
K
Karl-Johan Lindner, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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