De-escalation of Empirical Antimicrobial Therapy Study in Severe Sepsis
Primary Purpose
Severe Sepsis
Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
continuation of the empirical antimicrobial therapy
streamlining of the empirical antimicrobial therapy
Sponsored by
About this trial
This is an interventional treatment trial for Severe Sepsis
Eligibility Criteria
Inclusion Criteria:
- Major Subject;
- Subject having a sepsis engraves(burns) defined according to the following criteria during the initiation of the probability antibiotic treatment:
- Criteria of SIRS [ 14 ],
- And a suspected infection,
- And a failure of organ: low blood pressure, respiratory failure, coma, hepatic insufficiency, renal insufficiency, thrombopénia, spontaneous extension of the TCA,
- Subject for which an antibiotic treatment was begun within 6 hours following the diagnosis of sepsis engraves(burns);
- Subject for which a taking with microbiological aim was made within 48 hours following the diagnosis of sepsis
Exclusion Criteria:
- Minor Subject, pregnant or breast-feeding woman;
- Neutropénia (PN < 1000 / mm3);
- Absence of identification of a microorganism in the microbiological examinations;
- Absence of Social Security;
- Subject deprived of freedom or under guardianship;
- Subject for which the lit(enlightened) consent is not collected(taken in) (itself and/or reliable person).
Sites / Locations
- Assistance Publique Hopitaux de Marseille
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
a strategy based on de-escalation
a conservative strategy
Arm Description
Outcomes
Primary Outcome Measures
the length of stay
he deadline in days sold enters the diagnosis of sepsis engrave or toxic shock and the exit of resuscitation.
Secondary Outcome Measures
Mortality in resuscitation
The arisen of the death during the initial phase of stay in resuscitation
Lasted treatment antibiotic
Deadline in days between the beginning of the initiation of the treatment(processing) antibiotic and the 1st day when the subject is not any more handled by antibiotic
Lasted mechanical ventilation(breakdown)
Deadline in days sold between the implementation and the stop(ruling) of the mechanical ventilation(breakdown)
Lasted administration of catécholamines
The number of days without catécholamines during the stay in resuscitation
Full Information
NCT ID
NCT01626612
First Posted
June 4, 2012
Last Updated
April 20, 2015
Sponsor
Assistance Publique Hopitaux De Marseille
1. Study Identification
Unique Protocol Identification Number
NCT01626612
Brief Title
De-escalation of Empirical Antimicrobial Therapy Study in Severe Sepsis
Official Title
De-escalation of Empirical Antimicrobial Therapy Study in Severe Sepsis: A Randomized Clinical Trial (DEA Study)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
February 2012 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
July 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique Hopitaux De Marseille
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Rational: Severe sepsis is one of the leading cause of mortality in intensive care unit patients. Early initiation of an appropriate empirical antimicrobial therapy is associated with improved outcomes. In order to avoid an increase of selection pressure and the emergence of multidrug resistant pathogens, guidelines recommend to streamline the antimicrobial therapy after the identification of the pathogen responsible for infection. This strategy has been evaluated in several observational studies. However, at the bedside, few randomized clinical trials tested this strategy prospectively.
Method: the investigators conduct a randomized clinical trial comparing a strategy based on de-escalation (streamlining of the empirical antimicrobial therapy) and a conservative strategy (continuation of the empirical antimicrobial therapy). The investigators first aim was to show that a strategy based on de-escalation is not inferior to a conservative strategy in terms of intensive care unit length of stay. Secondary aims are to compare the rate of mortality rate, the emergence of multidrug resistant pathogens, and the feasibility of de-escalation. The study is performed in nine intensive care units from four institutions, and 120 patients are required to validate the investigators hypothesis. New technologies for the rapid diagnosis of severe infections are investigated in an ancillary study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Sepsis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)
8. Arms, Groups, and Interventions
Arm Title
a strategy based on de-escalation
Arm Type
Experimental
Arm Title
a conservative strategy
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
continuation of the empirical antimicrobial therapy
Intervention Description
ALL THE ANTIBACTERIAL IN WORN SYSTEMATIC
Intervention Type
Procedure
Intervention Name(s)
streamlining of the empirical antimicrobial therapy
Intervention Description
ALL THE ANTIBACTERIAL IN WORN SYSTEMATIC
Primary Outcome Measure Information:
Title
the length of stay
Description
he deadline in days sold enters the diagnosis of sepsis engrave or toxic shock and the exit of resuscitation.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Mortality in resuscitation
Description
The arisen of the death during the initial phase of stay in resuscitation
Time Frame
24 months
Title
Lasted treatment antibiotic
Description
Deadline in days between the beginning of the initiation of the treatment(processing) antibiotic and the 1st day when the subject is not any more handled by antibiotic
Time Frame
24 MONTHS
Title
Lasted mechanical ventilation(breakdown)
Description
Deadline in days sold between the implementation and the stop(ruling) of the mechanical ventilation(breakdown)
Time Frame
24 months
Title
Lasted administration of catécholamines
Description
The number of days without catécholamines during the stay in resuscitation
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Major Subject;
Subject having a sepsis engraves(burns) defined according to the following criteria during the initiation of the probability antibiotic treatment:
Criteria of SIRS [ 14 ],
And a suspected infection,
And a failure of organ: low blood pressure, respiratory failure, coma, hepatic insufficiency, renal insufficiency, thrombopénia, spontaneous extension of the TCA,
Subject for which an antibiotic treatment was begun within 6 hours following the diagnosis of sepsis engraves(burns);
Subject for which a taking with microbiological aim was made within 48 hours following the diagnosis of sepsis
Exclusion Criteria:
Minor Subject, pregnant or breast-feeding woman;
Neutropénia (PN < 1000 / mm3);
Absence of identification of a microorganism in the microbiological examinations;
Absence of Social Security;
Subject deprived of freedom or under guardianship;
Subject for which the lit(enlightened) consent is not collected(taken in) (itself and/or reliable person).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
BERNARD BELAIGUES
Organizational Affiliation
Assistance Publique hôpitaux de Marseille
Official's Role
Study Director
Facility Information:
Facility Name
Assistance Publique Hopitaux de Marseille
City
Marseille
ZIP/Postal Code
13354
Country
France
12. IPD Sharing Statement
Learn more about this trial
De-escalation of Empirical Antimicrobial Therapy Study in Severe Sepsis
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