Pharmacokinetics of Piperacillin and Meropenem in ICU Patients

  • STATUS
    Recruiting
  • End date
    Dec 31, 2023
  • participants needed
    50
  • sponsor
    Karolinska University Hospital
Updated on 2 December 2021

Summary

The purpose of the study is to characterize the pharmacokinetics of meropenem and piperacillin in ICU-patients at the time of the first dose administration and to contrast that with the same measurements obtained in the same patient 2-3 days later during the course of ICU treatment.

Details
Condition Antibiotic Pharmacokinetics
Treatment Piperacillin/tazobactam, Meropenem
Clinical Study IdentifierNCT05134298
SponsorKarolinska University Hospital
Last Modified on2 December 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patient being treated in one of the participating ICUs and planned to recieve treatment with meropenem or piperacillin
Exclusion Criteria (fullfilling any exlusion criteria means that patient
cannot be included in the study)
Not possible to retrospectively ask the patient or next of kin for consent to take part in the study or patient or next-of-kin not providing consent
Not posisble to obtain and process blood samples as specified by protocol
Ongoing renal replacement therapy
Patient having received the same antibiotic within the previous 96 h
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note