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Diagnosis of Septicaemia by Detection of Microbial DNA in Blood in Severe Infections (EVAMICA)

Primary Purpose

Febrile Neutropenia, Endocarditis, Severe Sepsis

Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Detection of microbial DNA in blood by SeptiFast®
detection of microbial DNA in blood by blood culture
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Febrile Neutropenia focused on measuring bacteria, fungi, real time PCR, adequate antimicrobial therapy, microbial DNA, microbial diagnosis

Eligibility Criteria

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

Inclusion Criteria:

  • Age≥ 18 years
  • Written signed and dated inform consent
  • First time with fever observed in a neutropenic patient
  • Severe sepsis in a patient hospitalized in ICU
  • Suspicion of infective endocarditis
  • Microbial investigation from Monday to Friday

Exclusion Criteria:

  • Not affiliated to Health Insurance (social security)
  • Included in another interventional trial testing microbial DNA detection during the time "without Septifast®"
  • Included in another clinical trial for which the clinician assumes that it will not be possible to prescribe an anti-infectious therapy adequately to microbial detection in the blood
  • Patient previously included in the protocol
  • Sepsis with a microbial diagnosis

Sites / Locations

  • CHU Henri Mondor

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

2

1

Arm Description

Detection by blood culture

Test LightCycler SeptiFast® (Roche)

Outcomes

Primary Outcome Measures

Number of bacteraemia and of fungemia - overall - each condition

Secondary Outcome Measures

Number of patients with adequate anti-infective therapy
Adequate anti-infective therapy
Time between sampling for microbial investigation and positive results relevant for the diagnosis
Mortality
Sepsis chock, secondary infectious focus
For neutropenia cases, number of patients who evaluated with a clinical focus of infection
Diagnosis of endocarditis
Number of non clinical investigations (microbial and non microbial)
Length of hospital stay

Full Information

First Posted
July 2, 2008
Last Updated
December 26, 2011
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Hoffmann-La Roche
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1. Study Identification

Unique Protocol Identification Number
NCT00709358
Brief Title
Diagnosis of Septicaemia by Detection of Microbial DNA in Blood in Severe Infections
Acronym
EVAMICA
Official Title
Health Economic Evaluation of Rapid Detection of Bacteraemia and Fungemia by Real Time PCR for Cases of Febrile Neutropenia, Suspicion of Endocarditis and Severe Sepsis in Intensive Care Units
Study Type
Interventional

2. Study Status

Record Verification Date
May 2011
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
September 2010 (Actual)
Study Completion Date
September 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Hoffmann-La Roche

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary purpose is to improve and quicken the microbial diagnosis in severe infections, since only one third of the cases are documented by blood cultures and adequate anti-infective therapy in the 48 hours reduced mortality and morbidity. Our hypothesis is that detection of microbial DNA in blood by real time PCR may increase the number of cases diagnosed for bacteraemia or fungemia and shorten the time to positive results, which will provide information for an adequate anti-infectious therapy.
Detailed Description
We will evaluate the advantage of adding the molecular test to the microbial investigations usually done (blood cultures and others) in cases of febrile neutropenia, suspicion of infective endocarditis and severe sepsis in intensive care units. This is a prospective study conducted in 18 sites (7 in the Paris area and 11 all over France) which will enrolled about 2000 patients over 18 years. Sites are randomized for starting with a 6-month period performing the test or 6-month period without the test (control time with the standard of care). Primary outcome are the number of patients with documented bacteraemia or fungemia. Secondary outcome are (1) the number of patients with an adequate anti-infective therapy and how long it happens after the diagnosis, (2) mortality, (3) new complicated infection, (4) number of investigations (microbial and non microbial) done for the etiological diagnosis, and global hospitalization costs. The advantage of the new test will be evaluated per protocol and with an intend to treat analyses. We hypothesized that the new test will bring 15% more microbial diagnosis than the standard of care. Consequently, and according to the number of sites interested in the study, 166 to 2500 patients will be enrolled with 480 to 750 patients with febrile neutropenia, 1000 to 1500 patients with severe sepsis in Intensive Care Units (ICU). Patients with suspicion of infective endocarditis will be evaluated for the number of diagnosis of true endocarditis according to Duke Criteria, and the time to diagnosis. Health economic evaluation will compare the costs of hospitalization, microbial investigations including the new test, other non clinical investigations and consequences on the organization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Febrile Neutropenia, Endocarditis, Severe Sepsis
Keywords
bacteria, fungi, real time PCR, adequate antimicrobial therapy, microbial DNA, microbial diagnosis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2000 (Actual)

8. Arms, Groups, and Interventions

Arm Title
2
Arm Type
Active Comparator
Arm Description
Detection by blood culture
Arm Title
1
Arm Type
Experimental
Arm Description
Test LightCycler SeptiFast® (Roche)
Intervention Type
Other
Intervention Name(s)
Detection of microbial DNA in blood by SeptiFast®
Intervention Description
The LightCycler® SeptiFast Test, the innovative real-time PCR test from Roche Diagnostics, is designed to detect and identify the 25 most important bacterial and fungal species causing bloodstream infections within just a few hours. The LightCycler® SeptiFast Test detects the pathogenic bacteria and fungi directly from whole blood without the need for prior incubation or culture steps. Rapid detection and identification of bacterial and fungal DNA, directly from a 1.5 ml whole blood sample, without prior incubation or culture steps in less than 6 hours.
Intervention Type
Other
Intervention Name(s)
detection of microbial DNA in blood by blood culture
Intervention Description
A blood culture is a test to find an infection in the blood. Most bacteria can be seen in the culture in 2 to 3 days, but some types can take 10 days or longer to show up. Fungus can take up to 30 days to show up in the culture.
Primary Outcome Measure Information:
Title
Number of bacteraemia and of fungemia - overall - each condition
Time Frame
max Day 30
Secondary Outcome Measure Information:
Title
Number of patients with adequate anti-infective therapy
Time Frame
at day 30
Title
Adequate anti-infective therapy
Time Frame
at 24h, 48h, > 48h
Title
Time between sampling for microbial investigation and positive results relevant for the diagnosis
Time Frame
between sampling for microbial investigation and positive results
Title
Mortality
Time Frame
at Day 30
Title
Sepsis chock, secondary infectious focus
Time Frame
at Day 30
Title
For neutropenia cases, number of patients who evaluated with a clinical focus of infection
Time Frame
at day 30
Title
Diagnosis of endocarditis
Time Frame
at Day 45
Title
Number of non clinical investigations (microbial and non microbial)
Time Frame
at day 30
Title
Length of hospital stay
Time Frame
at day 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age≥ 18 years Written signed and dated inform consent First time with fever observed in a neutropenic patient Severe sepsis in a patient hospitalized in ICU Suspicion of infective endocarditis Microbial investigation from Monday to Friday Exclusion Criteria: Not affiliated to Health Insurance (social security) Included in another interventional trial testing microbial DNA detection during the time "without Septifast®" Included in another clinical trial for which the clinician assumes that it will not be possible to prescribe an anti-infectious therapy adequately to microbial detection in the blood Patient previously included in the protocol Sepsis with a microbial diagnosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emmanuelle CAMBAU, PH
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
René COURCOL, PH
Organizational Affiliation
CHRU LILLE
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Henri Mondor
City
Créteil
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
28374097
Citation
Cambau E, Durand-Zaleski I, Bretagne S, Brun-Buisson C, Cordonnier C, Duval X, Herwegh S, Pottecher J, Courcol R, Bastuji-Garin S; EVAMICA study team. Performance and economic evaluation of the molecular detection of pathogens for patients with severe infections: the EVAMICA open-label, cluster-randomised, interventional crossover trial. Intensive Care Med. 2017 Nov;43(11):1613-1625. doi: 10.1007/s00134-017-4766-4. Epub 2017 Apr 3.
Results Reference
derived

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Diagnosis of Septicaemia by Detection of Microbial DNA in Blood in Severe Infections

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