Point of Care Evaluation of Fibrinolysis in Sepsis
NCT06312488
Critical Illness, Disease Attributes
Milan, MI, Italy
View Trial DetailsNCT Number: NCT04755777
The purpose of the study is to characterize various healthcare practitioners' perspectives on implementation of beta-lactam therapeutic drug monitoring in critical care practice.
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Notify Me18 year and older
All sexes
Observational
Royal Brisbane and Women's Hospital, Herston, Queensland, Australia
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Baseline
Indication of how many critically ill patients treated with beta-lactams should receive TDM.
Time frame: Baseline
Indication of which types of critically ill patients treated with beta-lactams should receive TDM
Time frame: Baseline
List of factors associated with successful beta-lactam TDM implementation
Mayo Clinic
Other
Provider Perspectives on Beta-lactam Therapeutic Drug Monitoring Programs in the Critically Ill: a Multicenter Mixed-methods Study
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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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