About this trial
ntra-abdominal candidiasis is a serious infection common in critically ill patients, often leading to high mortality if not treated quickly. Standard antifungal treatments may be less effective due to growing resistance and poor drug penetration into the abdominal cavity. In critically ill patients, drug levels can vary widely due to factors like surgery, inflammation, fluid resuscitation, or extracorporeal support, increasing the risk of underdosing. Rezafungin is a new antifungal agent with a long half-life and broad activity against Candida species, offering potential advantages in this setting. However, there is currently no data on its concentration or effectiveness in the peritoneal fluid of patients with intra-abdominal sepsis. Its long half-life, coupled with repeated pharmacokinetic variations in critical care settings and the risk of insufficient concentrations, may hinder its use in this population.
Eligibility criteria
Qualifiers
age > 18 years
with a suspected intra-abdominal candidiasis requiring abdominal surgery
and receiving the administration of rezafungin as first-line empirical antifungal treatment just before or within 1 hour the abdominal surgery
and having abdominal drain for at least 2 days after the surgery
Disqualifiers
death expected within 24h
decline to participate
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Central Hospital, Nancy, France
Lead sponsor
Mundipharma Research GmbH & Co KG
Collaborator