Rezafungin Peritoneal Diffusion for Intra-abdominal Candidiasis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentral Hospital, Nancy, France

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

20 Participants
are grouped into 1 trial group

Sponsors and collaborators

Central Hospital, Nancy, France

Lead sponsor

Mundipharma Research GmbH & Co KG

Collaborator