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Candida in the Respiratory Tract Secretions of Critically Ill Patients and The Efficacy of Antifungal Treatment (CANTREAT)

Primary Purpose

Ventilator Associated Pneumonia, Respiratory Tract Infection

Status
Terminated
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Normal Saline
anidulafungin
Sponsored by
Daren K. Heyland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Ventilator Associated Pneumonia focused on measuring Candida, ventilator associated pneumonia, respiratory tract infection, antifungal, biomarker

Eligibility Criteria

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

Inclusion Criteria:

  1. Adult patients (>18 years old)
  2. In the ICU > 48 hours
  3. Mechanically ventilated (>48 hours)
  4. Grow a Candida spp. on respiratory tract secretion culture (either by Bronchoalveolar Lavage or Endotracheal Aspirate) taken on or between 48 hours before or after the day of their suspicion of respiratory tract infection.
  5. Develop a clinical suspicion of respiratory tract infection while ventilated as defined by the following criteria (as defined previously in our VAP trial)5:

    • The presence of new, worsening or persistent radiographic features suggestive of pneumonia without another obvious cause AND
    • The presence of any two of the following:

      • Fever > 38C (core temperature)
      • Leukocytosis (>11.0 x109/L) or neutropenia (<3.5 x109/L)
      • Purulent endotracheal aspirates or change in character of aspirates
      • Isolation of pathogenic bacteria from endotracheal aspirates
      • Increasing oxygen requirements

Exclusion Criteria:

  1. Patients not expected to be in ICU for more than 72 hours (due to imminent death, withdrawal of aggressive care or discharge).
  2. Patients with Candida spp. in the blood or another sterile body site.
  3. Patients colonized at other non-pulmonary body site(s) with Candida.
  4. Already being treated with antifungal drugs (because of documented fungal infection, pre-emptive therapy, or prophylaxis).
  5. Allergy to study drugs (Fluconazole or the Echinocandin on formulary at treating institution).
  6. Immunocompromised patients (post-organ transplantation, Acquired Immunodeficiency Syndrome [AIDS], neutropenia [<1000 absolute neutrophils], corticosteroids [>20 mgs/day of prednisone or equivalent for more than 6 months]). These patients are excluded since Candida may be more invasive and these patients are much more likely to require systemic antifungal therapy.
  7. Patients with fulminant liver failure or end stage liver disease (Child's Class C).
  8. Women who are pregnant or lactating.
  9. Enrollment in industry sponsored interventional trial (co-enrollment in other academic studies would be allowed with the proviso that there was no potential interaction between the protocols).
  10. Prior randomization in this study.

Sites / Locations

  • Hamilton Health Sciences Centre
  • Kingston General Hospital
  • Ottawa General Hospital
  • Hopital Maisonneuve-Rosemont
  • Hopital du Sacre-Coeur do Montreal
  • Hopital l'Enfant-Jesus

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Antifungal

Arm Description

Saline will serve as the placebo solution since the active comparator is clear and colourless.

Patient will receive a dose daily for a total of 14 days

Outcomes

Primary Outcome Measures

Overall Recruitment Rate
Overall recruitment rate per site

Secondary Outcome Measures

Duration of Stay in ICU
Measure of the duration of participant stay in the ICU
Ventilator Free Days
Number of days in ICU free of ventilation
ICU Free Days
Number of days free of ICU
Antibiotic Free Days 28-day Post Randomization
Number of days free of antibiotic use within the first 28 days
Hospital Length of Stay
Measure of the duration of the participant's hospital stay
(SOFA) Post Randomization
Sequential organ failure assessment. 0-24 The higher the number the more severe organ failure
Sequential Procalcitonin
C-reactive Protein
Interleukin-6
B-glucan Levels

Full Information

First Posted
July 7, 2009
Last Updated
January 28, 2021
Sponsor
Daren K. Heyland
Collaborators
The Physicians' Services Incorporated Foundation, Queen's University, Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT00934934
Brief Title
Candida in the Respiratory Tract Secretions of Critically Ill Patients and The Efficacy of Antifungal Treatment
Acronym
CANTREAT
Official Title
Candida in the Respiratory Tract Secretions of Critically Ill Patients and The Efficacy of Antifungal Treatment (The CANTREAT Study): A Prospective, Randomized, Double Blind, Placebo Controlled Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Terminated
Why Stopped
slow enrollment
Study Start Date
April 2010 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Daren K. Heyland
Collaborators
The Physicians' Services Incorporated Foundation, Queen's University, Pfizer

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to determine whether the effect of treating Candida spp. isolated in the respiratory tract secretions of patients with a clinical suspicion of ventilator associated pneumonia (VAP) on clinical outcomes will be feasible and supported by biomarker data obtained.
Detailed Description
Candida spp. is commonly retrieved from microbiologic specimens of ICU patients with suspected VAP. It has been associated with increased systemic inflammation and worse clinical outcomes. This association may be due to the propensity for Candida to colonize those who are sicker, who have increased levels of systemic inflammation and worse clinical outcomes. However, an alternate possibility is that Candida is more than a colonizer and is responsible for the clinical and biochemical features observed. The only way to clarify the pathogenic role of Candida from this patient population is to treat the organism and see if patients improve compared to an untreated group. The purpose of this research program is to conduct such a study to determine if Candida in respiratory tract secretions should be routinely treated in critically ill patients. Since a definitive randomized controlled trial designed to demonstrate a reduction in mortality would be large, require the commitment of large amount of resources including both time and money, the investigators propose to first conduct a small pilot feasibility study. Eligible patients will be randomized to receive antifungal treatment with anidulafungin or placebo. Following enrollment, study treatment (or placebo) will be started as soon as possible. When the Candida or yeast organisms have been speciated and/or a susceptibility profile is known, the study medication will be adjusted based on susceptibility patterns. The investigators propose to treat with antifungal therapy for a total of 14 days. Patients will be followed daily for their entire stay in ICU or till day 28, whichever comes first. For patients discharged from the ICU to the ward, they will be followed until study treatment is complete (i.e. day 14). Mortality will be determined for the ICU stay, hospital stay and at 90 days. The investigators will record admission and discharge dates to ICU, step down units, and to hospital. All patients will have 13 mL of blood/day drawn at baseline, day 3, day 8 and at the end of the treatment period on day 14 (or last day of treatment). The samples will be prepared on site and shipped to a central lab for processing. The investigators will use the blood specimens to measure markers of inflammation (C-reactive protein, Procalcitonin, and Interleukin-6 and others as determined by the investigators), markers of candida presence (b-glucan and other potential future markers) and markers of immune dysfunction (to be determined by investigators).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventilator Associated Pneumonia, Respiratory Tract Infection
Keywords
Candida, ventilator associated pneumonia, respiratory tract infection, antifungal, biomarker

7. Study Design

Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
61 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Saline will serve as the placebo solution since the active comparator is clear and colourless.
Arm Title
Antifungal
Arm Type
Active Comparator
Arm Description
Patient will receive a dose daily for a total of 14 days
Intervention Type
Other
Intervention Name(s)
Normal Saline
Intervention Description
Normal Saline
Intervention Type
Drug
Intervention Name(s)
anidulafungin
Other Intervention Name(s)
TBA
Intervention Description
TBA
Primary Outcome Measure Information:
Title
Overall Recruitment Rate
Description
Overall recruitment rate per site
Time Frame
32 months
Secondary Outcome Measure Information:
Title
Duration of Stay in ICU
Description
Measure of the duration of participant stay in the ICU
Time Frame
28 days
Title
Ventilator Free Days
Description
Number of days in ICU free of ventilation
Time Frame
28 days
Title
ICU Free Days
Description
Number of days free of ICU
Time Frame
28 days
Title
Antibiotic Free Days 28-day Post Randomization
Description
Number of days free of antibiotic use within the first 28 days
Time Frame
28 days
Title
Hospital Length of Stay
Description
Measure of the duration of the participant's hospital stay
Time Frame
90 days
Title
(SOFA) Post Randomization
Description
Sequential organ failure assessment. 0-24 The higher the number the more severe organ failure
Time Frame
post randomization
Title
Sequential Procalcitonin
Time Frame
28 days
Title
C-reactive Protein
Time Frame
28 days
Title
Interleukin-6
Time Frame
28 days
Title
B-glucan Levels
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients (>18 years old) In the ICU > 48 hours Mechanically ventilated (>48 hours) Grow a Candida spp. on respiratory tract secretion culture (either by Bronchoalveolar Lavage or Endotracheal Aspirate) taken on or between 48 hours before or after the day of their suspicion of respiratory tract infection. Develop a clinical suspicion of respiratory tract infection while ventilated as defined by the following criteria (as defined previously in our VAP trial)5: The presence of new, worsening or persistent radiographic features suggestive of pneumonia without another obvious cause AND The presence of any two of the following: Fever > 38C (core temperature) Leukocytosis (>11.0 x109/L) or neutropenia (<3.5 x109/L) Purulent endotracheal aspirates or change in character of aspirates Isolation of pathogenic bacteria from endotracheal aspirates Increasing oxygen requirements Exclusion Criteria: Patients not expected to be in ICU for more than 72 hours (due to imminent death, withdrawal of aggressive care or discharge). Patients with Candida spp. in the blood or another sterile body site. Patients colonized at other non-pulmonary body site(s) with Candida. Already being treated with antifungal drugs (because of documented fungal infection, pre-emptive therapy, or prophylaxis). Allergy to study drugs (Fluconazole or the Echinocandin on formulary at treating institution). Immunocompromised patients (post-organ transplantation, Acquired Immunodeficiency Syndrome [AIDS], neutropenia [<1000 absolute neutrophils], corticosteroids [>20 mgs/day of prednisone or equivalent for more than 6 months]). These patients are excluded since Candida may be more invasive and these patients are much more likely to require systemic antifungal therapy. Patients with fulminant liver failure or end stage liver disease (Child's Class C). Women who are pregnant or lactating. Enrollment in industry sponsored interventional trial (co-enrollment in other academic studies would be allowed with the proviso that there was no potential interaction between the protocols). Prior randomization in this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daren Heyland, MD
Organizational Affiliation
Clinical Evaluation Research Unit
Official's Role
Study Chair
Facility Information:
Facility Name
Hamilton Health Sciences Centre
City
Hamilton
State/Province
Ontario
Country
Canada
Facility Name
Kingston General Hospital
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 2V7
Country
Canada
Facility Name
Ottawa General Hospital
City
Ottawa
State/Province
Ontario
Country
Canada
Facility Name
Hopital Maisonneuve-Rosemont
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H1T 2M4
Country
Canada
Facility Name
Hopital du Sacre-Coeur do Montreal
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4J 1C5
Country
Canada
Facility Name
Hopital l'Enfant-Jesus
City
Quebec
ZIP/Postal Code
G1J 1Z4
Country
Canada

12. IPD Sharing Statement

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Candida in the Respiratory Tract Secretions of Critically Ill Patients and The Efficacy of Antifungal Treatment

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