ICCA: Early Identification of Candida in Intra-abdominal Candidiasis

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Recruiting
CT.gov ID
NCT05264571
Collaborator
SYMCEL (Other)
100
1
3.3
30.4

Study Details

Study Description

Brief Summary

Intra-abdominal candidiasis remains the first origin of invasive candidiasis in critically ill patients with a mortality up to 60%. This high mortality is partly related to delay of anti-fungal treatment administration. According to experts in the field, new diagnostic methods to rapidly detect Candida in intra-abdominal infections is mandatory because the current strategies suffer from a lack of both sensitivity and specificity.

The calscreener (SYMCEL®) is a new diagnostic tool to rapidly identify the presence of pathogens in biological samples based on micrometabolic activity detection.

The ICCA project will test the feasibility, the accuracy and the diagnostic performance of the calscreener on an existing biological collection of peritoneal fluid. This collection came from a cohort of critically ill patients with intra-abdominal infection which required abdominal surgery. Intra-abdominal infections consist of bacterial peritonitis and intra-abdominal candidiasis. The presence of pathogens (bacteria and yeast) is already known, the peritoneal fluid being stored after routine analysis (bacteriology / mycology).

Only the detection / identification of yeast will be investigated in this project.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: calscreener

Detailed Description

The high mortality rate of patients with intra-abdominal candidiasis infection is partly related to delay in anti-fungal treatment. The gold standard method for Candida detection remains the yeast culture on mycological media which suffers from a delayed response time (up to 5 days).

Consequently, in the routine practice, the decision to start an anti-fungal treatment is based on predictive scores such as the Peritonitis score. Whatever the score, they all suffer from a lack of sensitivity and specificity and could expose ICU patients to delayed treatment with negative impact on mortality. Once introduced and before the availability of the result of the culture, the anti-fungal can be stopped based on two serum measures of 1,3 beta D Glucan < 80 pg/ml. This strategy allows anti-fungal spare. Therefore, there is a room for improvement regarding early Candida detection and identification for the right choice of anti-fungal.

The calscreener (SYMCEL®) is a new diagnostic tool to rapidly identify the presence of pathogens in biological samples based on micrometabolic activity detection. The metabolic activity anticipates the future positive culture. To date, most of the experiments with the calscreenerTM concern bacteria. During the development phase, some experiments have been performed with Candida, mostly in vitro. Data of feasibility with clinical samples such as the peritoneal fluid are lacking. Besides, there is currently no library regarding the metabolic profile of Candida, in both albicans and non-albicans species. All in all, its routine use is currently impossible.

First results (unpublished data from our team) of metabolic activity detection in peritoneal fluid with known presence of Candida showed a time detection <1 hour. We aim to confirm these promising results using biological samples collected in an ongoing cohort study. We first need to describe the metabolic activity curves of different Candida species in order to constitute a library.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
The ICCA Study (Early Identification of Candida in Intra-abdominal CAndidiasis)
Actual Study Start Date :
Feb 17, 2022
Anticipated Primary Completion Date :
Apr 28, 2022
Anticipated Study Completion Date :
May 28, 2022

Arms and Interventions

Arm Intervention/Treatment
critically ill adult patients with intra-abdominal infection

The ICCA study is an ancillary study of a non-interventional prospective cohort study (the pBDG2 study, NCT03997929) The pBDG 2 study has enrolled ICU patients with intra-abdominal infection requiring abdominal surgery. During the surgery, peritoneal fluid has been collected to identify the pathogens involved and guide anti-infective therapies. After the routine analyses, the remained peritoneal fluid was stored to create a biological collection. This biological collection, in which the content of bacterias and yeasts is known, will be analysed with the calscreener.

Diagnostic Test: calscreener
The calscreener (SYMCEL®) is a new diagnostic tool to rapidly identify the presence of pathogens in biological samples based on micrometabolic activity detection. All living cells produce heat by the chemical and physical processes of life; by monitoring the heat flow over time (J/s, W) a significant amount of information can be obtained regarding the biological system.

Outcome Measures

Primary Outcome Measures

  1. Detection (Yes/No) of the presence of Candida in the peritoneal fluid [Day 1 - 3]

    Detection by the calscreener : detection of metabolic activity > 5 µW (according to SYMCEL recommendation)

Secondary Outcome Measures

  1. Delay (in hours) of detection [Day 1 - 3]

    Delay (in hours) from the start of calscreener analysis to first detection of heat flow > 5 µW

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

The criteria belong to the pBDG2 study (Peritoneal 1.3-ß-D-glucan for the Diagnosis of Intra-abdominal Candidiasis in Critically Ill Patients).

Inclusion Criteria:
  • adult

  • Covered by health insurance

  • Admitted in ICU with intra-abdominal infection requiring abdominal surgery or percutaneous drainage

Exclusion Criteria:
  • Pregnant or lactating woman

  • Patient deprived of liberty after administration of juridical decision

  • Patient under psychiatric care

Contacts and Locations

Locations

Site City State Country Postal Code
1 Central Hospital Vandoeuvre les Nancy France 54500

Sponsors and Collaborators

  • Central Hospital, Nancy, France
  • SYMCEL

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT05264571
Other Study ID Numbers:
  • 2021PI051
First Posted:
Mar 3, 2022
Last Update Posted:
Mar 3, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Central Hospital, Nancy, France
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 3, 2022