Negative Beta Glucan in ICU Patients
Primary Purpose
Candidemia
Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Anidulafungin
Sponsored by
About this trial
This is an interventional treatment trial for Candidemia focused on measuring candidemia, intensive care unit, 1,3 beta-D-glucan
Eligibility Criteria
Inclusion Criteria:
In the ICU for >2 days AND
- Systemic antibiotics on days 1-3 of ICU OR
- Central venous catheter on days 1-3 of ICU
AND at least 2 of:
- Total parenteral nutrition on days 1-3 of ICU
- Any dialysis on days 1-3 of ICU
- Major surgery in the 7 days before admission in the ICU
- Pancreatitis in the 7 days before admission in the ICU
- Use of corticosteroids for at least 3 days in the 7 days before admission
- Use of other immunosuppressive agents in the 7 days before admission in the ICU
In addition, the patient must have at least one of the following:
- Fever (axillary temperature >37.5 oC)
- Hypothermia (axillary temperature <35 oC)
- Hypotension
- Unexplained acidosis
- Unexplained elevation in C-reactive protein
Exclusion Criteria:
- Antifungal for >3 days
- Allergy to an echinocandin
Sites / Locations
- Federal University of Rio de Janeiro
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Anidulafungin
Arm Description
Patients at risk will receive therapy with anidulafungin
Outcomes
Primary Outcome Measures
Evaluate the Ocurrence of Candidemia in Patients With Negative 1,3 Beta-D-glucan Who Discontinue Anidulafungin
The main interest is to evaluate the ocurrence of candidemia in patients with negative 1,3 beta-D-glucan who discontinue anidulafungin
Secondary Outcome Measures
Full Information
NCT ID
NCT01734525
First Posted
November 20, 2012
Last Updated
April 18, 2019
Sponsor
Universidade Federal do Rio de Janeiro
1. Study Identification
Unique Protocol Identification Number
NCT01734525
Brief Title
Negative Beta Glucan in ICU Patients
Official Title
A Pilot Study for the Use of Biomarkers and Early Treatment of Invasive Candidiasis in ICU Patients
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal do Rio de Janeiro
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a prospective study aimed at testing a strategy of early initiation of an antifungal agent to patients admitted to intensive care units (ICUs) at risk for invasive candidiasis. Score system have been developed to identify groups at very high risk for the development of candidemia/invasive candidiasis in the ICU. These scoring system have used clinical information with or without data on Candida colonization, and have shown reasonable correlation with candidemia/invasive candidiasis. More recently, a biomarker - detection of 1,3-beta-D-glucan in the serum - has been tested in the early diagnosis of candidiasis. The incorporation of biomarkers such as beta-D-glucan could help clinicians to select a group at higher risk for candidemia, and despite the fact that these tests may give false-positive results, their negative predictive value could be of great help.
Therefore, the objectives of this study are:
To assess the frequency of positive biomarkers in ICU patients at high risk to develop invasive candidiasis/candidemia;
To test the strategy of early discontinuation of antifungal therapy based on repeatedly negative blood cultures and 1,3 beta-D-glucan in the serum.
Detailed Description
Entry criteria are: In the ICU for >2 days AND systemic antibiotics >2 days OR central venous catheter for >days AND at least two of the following: total parenteral nutrition, dialysis, surgery, pancreatitis, receipt of corticosteroids, receipt of other immunosuppressive agents. In addition, patients must have a clinical sign of infection (either one of the following): fever, hypothermia, hypotension, unexplained acidosis, or unexplained elevation in C-reactive protein.
Eligible patients will be enrolled after signing an informed consent and will have blood obtained for culture and determination of 1,3 beta-D-glucan serum levels for 3 days, and will start anidulafungin IV.
If all tests are negative, anidulafungin will be discontinued on day 4. If 1,3 beta-D-glucan is positive (>80 pg/ml) and / or blood cultures are positive for Candida species, anidulafungin will be continued for >14 days.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Candidemia
Keywords
candidemia, intensive care unit, 1,3 beta-D-glucan
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
85 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Anidulafungin
Arm Type
Experimental
Arm Description
Patients at risk will receive therapy with anidulafungin
Intervention Type
Drug
Intervention Name(s)
Anidulafungin
Intervention Description
Anidulafungin at a dose of 200 mg in the first day and 100 mg daily afterwards
Primary Outcome Measure Information:
Title
Evaluate the Ocurrence of Candidemia in Patients With Negative 1,3 Beta-D-glucan Who Discontinue Anidulafungin
Description
The main interest is to evaluate the ocurrence of candidemia in patients with negative 1,3 beta-D-glucan who discontinue anidulafungin
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
In the ICU for >2 days AND
Systemic antibiotics on days 1-3 of ICU OR
Central venous catheter on days 1-3 of ICU
AND at least 2 of:
Total parenteral nutrition on days 1-3 of ICU
Any dialysis on days 1-3 of ICU
Major surgery in the 7 days before admission in the ICU
Pancreatitis in the 7 days before admission in the ICU
Use of corticosteroids for at least 3 days in the 7 days before admission
Use of other immunosuppressive agents in the 7 days before admission in the ICU
In addition, the patient must have at least one of the following:
Fever (axillary temperature >37.5 oC)
Hypothermia (axillary temperature <35 oC)
Hypotension
Unexplained acidosis
Unexplained elevation in C-reactive protein
Exclusion Criteria:
Antifungal for >3 days
Allergy to an echinocandin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcio Nucci, MD
Organizational Affiliation
Universidade Federal do Rio de Janeiro
Official's Role
Study Chair
Facility Information:
Facility Name
Federal University of Rio de Janeiro
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
21941913
Country
Brazil
12. IPD Sharing Statement
Citations:
PubMed Identifier
27287231
Citation
Nucci M, Nouer SA, Esteves P, Guimaraes T, Breda G, de Miranda BG, Queiroz-Telles F, Colombo AL. Discontinuation of empirical antifungal therapy in ICU patients using 1,3-beta-d-glucan. J Antimicrob Chemother. 2016 Sep;71(9):2628-33. doi: 10.1093/jac/dkw188. Epub 2016 Jun 10.
Results Reference
derived
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Negative Beta Glucan in ICU Patients
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