RecruitingNot ApplicableNCT03538912

Early Discontinuation of Empirical Antifungal Therapy and Biomarkers

Impact of the Use of Biomarkers on Early Discontinuation of Empirical Antifungal Therapy in Critically Ill Patients: a Randomized Controlled Study.


Sponsor

University Hospital, Lille

Enrollment

194 participants

Start Date

Jun 6, 2018

Study Type

INTERVENTIONAL

Conditions

Summary

Empirical antifungal therapy (EAT) is frequently prescribed to septic critically ill patients with risk factors for invasive Candida infections (ICI). However, among patients without subsequent proven ICI, antifungal discontinuation is rarely performed, resulting in unnecessary antifungal overuse. The investigators postulate that the use of fungal biomarkers could increase the percentage of early discontinuation of EAT among critically ill patients suspected of ICI, as compared with a standard strategy, without negative impact on day 28-mortality. To test this hypothesis, the investigators designed a randomized controlled open-label parallel-group study.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Patient older than 18 years
  • Who require EAT for the first time in the ICU (this treatment is prescribed based on the presence of risk factors and clinical suspicion of ICI)
  • With an expected ICU length of stay of at least 6 days after EAT initiation
  • Informed written consent

Exclusion Criteria6

  • Neutropenia (neutrophil count <500 cells /µL)
  • Active malignant hemopathy
  • Bone marrow transplantation in the last 6 months
  • Polyvalent immunoglobulins in the past months
  • Documented ICI in the past 3 months
  • Pregnancy or breastfeeding

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERBiomarker strategy

EAT duration is determined by β-D-1,3-glucan and mannan serum assays, performed at day 0 (day of EAT initiation) and day 3.

OTHERRoutine strategy

EAT duration is based on IDSA guidelines, which recommend 14 days of treatment for patients without subsequent proven ICI, and who improve under antifungal treatment, or less in other situations.


Locations(10)

CH ARRAS

Arras, France

CH de DOUAI

Douai, France

CH Dunkerque

Dunkirk, France

Centre Hospitalier Dr Schaffner

Lens, France

Ch Dr.Schaffner de Lens

Lens, France

Hôpital Roger Salengro, CHU

Lille, France

CH Roubaix

Roubaix, France

CHU de Rouen

Rouen, France

Ch Tourcoing

Tourcoing, France

Centre hospitalier de valenciennes

Valenciennes, France

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT03538912


Related Trials