Actively Recruiting

Phase 4
Age: 18Years +
All Genders
ID06848387

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Treating physician has decided to start continuous infusion of cloxacillin
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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

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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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