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Prolonged Infusion Cefepime and Nosocomial Infections (PICNIC)

Primary Purpose

Urinary Tract Infection, Respiratory Tract Infection

Status
Unknown status
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Prolonged Cefepime Infusion
Usual Cefepime Infusion
Sponsored by
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Tract Infection

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Urinary tract infection after 48-72 hours of hospital stay
  • Respiratory tract infection after 48-72 hours of hospital stay
  • Catheter related urinary tract infection after 48-72 hours of hospital stay
  • Urinary or respiratory infections not responding to a narrower spectrum antibiotic
  • Isolation of bacteria sensible to cefepime in blood, urine or sputum in a clinical context of infection

Exclusion Criteria:

  • Glomerular filtration rate lower than 30 ml.min/1,73m²
  • ICU admission for at least 72 hours before randomization
  • Neutrophil count lower than 1000 cels per mm³
  • Hematologic malignancy, bronchiectasis and cystic fibrosis
  • Patients allergic to cefepime
  • Concomitant treatment to another infectious disease
  • Central nervous system, cutaneous or intrabdominal infections
  • Solid organ transplantation
  • HIV with a cluster differentiation 4 (CD4) lower than 100 cels per mm³

Sites / Locations

  • Hospital de Clínicas de Porto AlegreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Prolonged Cefepime Infusion

Usual Cefepime Infusion

Arm Description

Cefepime infusions should last 4 hours at least

Cefepime infusion should last no more than 30 minutes

Outcomes

Primary Outcome Measures

Death
Death in 30 days since randomization

Secondary Outcome Measures

Death
Death in 14 days since randomization
Duration of hospital stay
Duration of hospital stay
Intensive care unit (ICU) admission
Intensive care necessity for any reason
Duration of intensive care unit (ICU) stay
Number of days when intensive care was considered necessary
Treatment change
Treatment change required based com clinical or microbiological data
Treatment success
Patient reaching the completion until it end with infection resolution
Time to clinical stability
Time required for patient to reach the normalization of all following vital signs: that is, body temperature lower than 37,9 degrees celsius, a cardiac rate lower than 100 beats per minute and a respiratory rate lower than 25 respiratory movements per minute and peripheral oxygen saturation higher than 91% with low oxygen requirement (that is 4 liters per minute delivered by nasal canula)

Full Information

First Posted
October 2, 2015
Last Updated
October 15, 2015
Sponsor
Hospital de Clinicas de Porto Alegre
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1. Study Identification

Unique Protocol Identification Number
NCT02568800
Brief Title
Prolonged Infusion Cefepime and Nosocomial Infections
Acronym
PICNIC
Official Title
Prolonged Infusion Cefepime and Nosocomial Infections
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
October 2015 (undefined)
Primary Completion Date
March 2016 (Anticipated)
Study Completion Date
September 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital de Clinicas de Porto Alegre

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
It is advocated that prolonged infusion of beta-lactamic antibiotics provides better bactericidal effect. The aim of the present study is to randomize patients a to extended cefepime infusion regimen (lasting four hours) or to a usual infusion regimen (not lasting more than thirty minutes) and evaluate the clinical efficacy of this theoretical pharmacokinetic advantage.
Detailed Description
Introduction: it has been proved that the main determinant for microbiological cure gram-negative infections treated with cefepime is the time above minimal inhibitory concentration (T>MIC). Although this particular pharmacokinetic property have never been proved in clinical trials utilizing cefepime, intervention studies with other betalactamic antibiotics, such as pipercillin-tazobactam, showed clinical benefit. Objective: to evaluate if prolonged infusion (lasting 4 hours) with cefepime translate into better clinical outcomes. Methods: the investigators aim to conduct an open-label, unique-centered, randomized controlled trial using cefepime in prolonged infusions in patients being treated for urinary or respiratory tract infections. Patients developing these infections after 72 hours of hospital admission, requiring the use of broader spectrum antibiotics after clinical failure or isolating gram-negative bacteria from adequate sample sensible to cefepime will be enrolled. The use of a second antibiotic such as clindamycin, vancomycin or metronidazole will be allowed. Interventions: the investigators aim to randomize 134 patients to two different treatment arms, the intervention arm who will receive the medication in a four hour lasting infusion, and the active control arm who will receive the medication in a 30 minutes lasting infusion. The randomization will be conducted in blocks of ten patients each, and it will be balance according to the patients age (older or younger than 65 years old) and presence of SIRS criteria.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infection, Respiratory Tract Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
134 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Prolonged Cefepime Infusion
Arm Type
Experimental
Arm Description
Cefepime infusions should last 4 hours at least
Arm Title
Usual Cefepime Infusion
Arm Type
Active Comparator
Arm Description
Cefepime infusion should last no more than 30 minutes
Intervention Type
Drug
Intervention Name(s)
Prolonged Cefepime Infusion
Other Intervention Name(s)
Estended Cefepime Infusion
Intervention Description
Cefepime infusion should last at least 4 hours with the aide of an infusion bomb
Intervention Type
Drug
Intervention Name(s)
Usual Cefepime Infusion
Other Intervention Name(s)
Regular Cefepime Infusion
Intervention Description
Cefepime infusion occurs directly without the aide of an infusion bomb, lasting roughly thirty minutes
Primary Outcome Measure Information:
Title
Death
Description
Death in 30 days since randomization
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Death
Description
Death in 14 days since randomization
Time Frame
14 days
Title
Duration of hospital stay
Description
Duration of hospital stay
Time Frame
30 days since randomization
Title
Intensive care unit (ICU) admission
Description
Intensive care necessity for any reason
Time Frame
30 days since randomization
Title
Duration of intensive care unit (ICU) stay
Description
Number of days when intensive care was considered necessary
Time Frame
30 days since randomization
Title
Treatment change
Description
Treatment change required based com clinical or microbiological data
Time Frame
3 days after randomization
Title
Treatment success
Description
Patient reaching the completion until it end with infection resolution
Time Frame
30 days since randomization
Title
Time to clinical stability
Description
Time required for patient to reach the normalization of all following vital signs: that is, body temperature lower than 37,9 degrees celsius, a cardiac rate lower than 100 beats per minute and a respiratory rate lower than 25 respiratory movements per minute and peripheral oxygen saturation higher than 91% with low oxygen requirement (that is 4 liters per minute delivered by nasal canula)
Time Frame
3 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Urinary tract infection after 48-72 hours of hospital stay Respiratory tract infection after 48-72 hours of hospital stay Catheter related urinary tract infection after 48-72 hours of hospital stay Urinary or respiratory infections not responding to a narrower spectrum antibiotic Isolation of bacteria sensible to cefepime in blood, urine or sputum in a clinical context of infection Exclusion Criteria: Glomerular filtration rate lower than 30 ml.min/1,73m² ICU admission for at least 72 hours before randomization Neutrophil count lower than 1000 cels per mm³ Hematologic malignancy, bronchiectasis and cystic fibrosis Patients allergic to cefepime Concomitant treatment to another infectious disease Central nervous system, cutaneous or intrabdominal infections Solid organ transplantation HIV with a cluster differentiation 4 (CD4) lower than 100 cels per mm³
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
André Dias Américo
Phone
+555193112207
Email
adamerico@hcpa.edu.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eduardo Sprinz
Organizational Affiliation
Hospita de Clínicas de Porto Alegre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de Clínicas de Porto Alegre
City
Porto Alegre
State/Province
Rio Grande do Sul
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
André Dias Américo
Phone
+555133598152
Email
adamerico@hcpa.edu.br

12. IPD Sharing Statement

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Prolonged Infusion Cefepime and Nosocomial Infections

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