Clinical Trials Directory

Trials / Completed

CompletedNCT01994096

Optimal Dosage of Caspofungin in Critically Ill Patients

Pharmacokinetics and Optimal Dosage of Caspofungin in Critically Ill Patients With Suspected Invasive Candidiasis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
20 (actual)
Sponsor
University Medical Center Groningen · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Intensive care unit (ICU) patients are especially at risk for invasive candidiasis due to the presence of risk factors. It is known that in critically ill patients, alterations in function of various organs and body systems can influence the pharmacokinetics and hence the plasma concentration of a drug. A study of caspofungin in ICU patients has found a high inter- and intra-individual variability in caspofungin concentration. Factors that caused subtherapeutic caspofungin plasma concentrations were body weight \> 75 kg and hypoalbuminemia. Furthermore, an efficacy study showed a lower response rate for caspofungin among patients with a higher disease severity score. As a result of the altered pharmacokinetics, under- or over-exposure of caspofungin can occur in critically ill patients and an adjusted dosage might be necessary in these patients.

Conditions

Interventions

TypeNameDescription
DRUGCaspofungin

Timeline

Start date
2013-11-01
Primary completion
2015-10-01
Completion
2015-10-01
First posted
2013-11-25
Last updated
2015-10-30

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01994096. Inclusion in this directory is not an endorsement.