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Clinical Trials/NCT02400268
NCT02400268
Completed
Phase 3

Phase 4, Randomized, Controlled Multicentric, Open-label Clinical Trial to Prove That the 7 Day Course of Treatment for Enterobacteriaceae Bacteremia is More Efficient and Equally Safe Than 14 Day Scheme

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla4 sites in 1 country238 target enrollmentSeptember 2014

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Enterobacteriaceae Infections
Sponsor
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
Enrollment
238
Locations
4
Primary Endpoint
Days of antimicrobial treatment
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The antimicrobial crisis is a real problem. Infections produced by multiresistant bacteria are becoming more and more frequent, and available antimicrobial agents are usually scarce. Reducing the duration of antimicrobial treatments is one of the most efficient measures to control the antibiotic pressure and to optimise the use of these agents.

Bloodstream infections produced by Enterobacteria (EB) are very frequent, but the optimal duration of antibiotics to treat them is unknown, as long as no clinical trials have been specifically developed to answer this question.

Basing on expert opinions, the Infectious Diseases Society pf America (IDSA) recommends the bacteremia by EB secondary to vascular catheter infections to be treated for 7 to 14 days. This represents a variability of up to 100%. No recommendations have been published regarding the duration of treatment of bacteremia from other sources.

The objective of this project is to prove that the 7-day course of treatment for EB bacteremia is more efficient and equally safe than the 14-day scheme.

Detailed Description

To achieve theses objectives, we propose this randomized, multicentric clinical trial with a superiority design on the duration of antimicrobial treatment for EB bacteremia in adult patients.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
March 1, 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Pregnancy
  • Post-chemotherapy neutropenia expected to persist more than 7 days.
  • Source of bacteremia uncontrolled at inclusion period or in the following 24 hours. The source will be considered as uncontrolled if the bacteremia is secondary to a suppurative infection potentially removable, if no action has been taken to eradicate it, including: bacteremia by vascular not removed catheter, cholangitis secondary to not derived obstruction of the biliary tract, deep abscess not drained, pyohydronephrosis without derivation of the urinary tract.
  • Bacteremia secondary to infective endocarditis, bone and joint infections, or neurosurgical infections, which may require prolonged antimicrobial therapy
  • Bacteremia due to enterobacteriaceae resistant to carbapenemics.
  • Polymicrobial bacteremia including microorganisms different to enterobacteriaceae.
  • Patients with no expectations of survival in the next 48 hours of inclusion.

Outcomes

Primary Outcomes

Days of antimicrobial treatment

Time Frame: 28 days

To prove that 7-days course of antibiotic therapy is more efficient than 14-days course when treating Enterobacteriaceae bacteremia, in terms of number of days at the end of follow up.

Secondary Outcomes

  • Adverse reactions related to antimicrobial treatment(28 days)
  • Cure of bacteremia(28 days)
  • Procalcitonin levels(7-days and 14-days)

Study Sites (4)

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