Status:

COMPLETED

Therapeutic Drug Monitoring of Antifungals in Intensive Care Units

Lead Sponsor:

Hospices Civils de Lyon

Conditions:

Intensive Care Unit Patients

Eligibility:

All Genders

16+ years

Brief Summary

Antifungals under- and over-dosing are frequently deplored in patients treated with antifungals and receiving recommended doses, mostly in critically-ill patients. This situation is well-described for...

Eligibility Criteria

Inclusion

  • Adult patients who received antifungals including fluconazole, voriconazole, posaconazole, or caspofungin, during their ICU stay and had a Therapeutic Drug Monitoring (TDM)

Exclusion

  • Patients without antifungal treatment
  • Patients who received an antifungal combination
  • Pediatric patients
  • Patients who were not admitted in ICU
  • Patients who did not have a TDM

Key Trial Info

Start Date :

January 1 2018

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 31 2019

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT04502771

Start Date

January 1 2018

End Date

December 31 2019

Last Update

August 7 2020

Active Locations (1)

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Hospices Civils de Lyon, Croix-Rousse Hospital

Lyon, France, 69004