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Negative Beta Glucan in ICU Patients

Primary Purpose

Candidemia

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Anidulafungin
Sponsored by
Universidade Federal do Rio de Janeiro
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
November 20, 2012
Last Updated
April 18, 2019
Sponsor
Universidade Federal do Rio de Janeiro
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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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