Rezafungin Peritoneal Diffusion for Intra-abdominal Candidiasis
Recruiting now
Conditions studied: Intra-Abdominal Infection, Candida, Abdominal Surgery Patients, Critically Ill Intensive Care Unit Patients
In brief
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.
Key facts
- Study ID
- NCT07093203
- Run by
- Central Hospital, Nancy, France
- People needed
- 20
- Starts
- 2025-11-14
- Expected to finish
- 2026-09-01
- Last updated by the study team
- 2026-04-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- death expected within 24h
- decline to participate
Where it is running
- CHRU de Nancy — Vandœuvre-lès-Nancy, Lorraine, France (enrolling)
Full record on ClinicalTrials.gov
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