search
Back to results

Seven Versus 14 Days of Antibiotic Therapy for Multidrug-resistant Gram-negative Bacilli Infections (OPTIMISE)

Primary Purpose

Carbapenem-Resistant Enterobacteriaceae Infection, Bloodstream Infection, Severe Infection

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Duration of therapy
Sponsored by
Hospital Moinhos de Vento
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carbapenem-Resistant Enterobacteriaceae Infection

Eligibility Criteria

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

Inclusion criteria

  • Patient admitted to the intensive care unit
  • Severe infection in any site (defined as the presence of sepsis/septic shock or bloodstream infection) associated with a positive culture by MRD-GNB (Acinetobacter baumannii complex, Pseudomonas aeruginosa, and Enterobacterales bacteria, only susceptible to carbapenems and/or polymyxins)
  • Hemodynamically stable and afebrile (axillary temperature less than 37.8ºC) for at least 48 hours on day 7 of adequate antibiotic therapy

Exclusion criteria

  • Inclusion in other experimental studies involving antimicrobial therapy
  • Infections that have as the primary site: endocarditis/endovascular infection, necrotizing fasciitis, osteomyelitis, abdominal abscess or other abdominal infections requiring surgical intervention, central nervous system infections, empyema, prosthetic infection
  • Immunosuppression defined as: neutrophil cells <1000/mm³ in the current hospitalization, HIV/AIDS diagnosis with last CD4 count <200/mm³, solid organ transplantation in the last year and/or need for increased immunosuppression due to acute rejection in the last year, hematopoietic stem cell transplantation in the last year, and/or current therapy for chronic graft-versus-host disease
  • Positive blood cultures for the same pathogen within 48 hours prior to randomization, when collected
  • Concomitant infection with another GNB (regardless of susceptibility profile)
  • Previous inclusion in this study
  • Known pregnancy

Sites / Locations

  • Hospital Cleriston de Andrade
  • Hospital Couto MaiaRecruiting
  • Hospital da CidadeRecruiting
  • Hospital OTO clinicaRecruiting
  • Instituto Hospital de Base do Distrito FederalRecruiting
  • Hospital Universitário de BrasíliaRecruiting
  • Hospital Evangélico de Vila VelhaRecruiting
  • Hospital Presidente VargasRecruiting
  • Santa Casa de Misericórdia de Belo Horizonte
  • Hospital Vila da Serra (Instituto Materno Infantil de Minas Gerais S/A)
  • Irmandade da Santa Casa de Misericórdia de PassosRecruiting
  • Hospital Universitário da Universidade Estadual de LondrinaRecruiting
  • Hospital Municipal de MaringáRecruiting
  • Hospital Regional Baixo Amazonas
  • Hospital do TricentenárioRecruiting
  • Hospital São João BatistaRecruiting
  • Hospital Tacchini
  • Hospital Geral Caxias do SulRecruiting
  • Hospital de Clinicas de Porto AlegreRecruiting
  • Hospital Ernesto DornellesRecruiting
  • Hospital Nossa Senhora da ConceiçãoRecruiting
  • Hospital São Lucas da PUCRecruiting
  • Hospital Santa Cruz
  • Hospital Ana NeryRecruiting
  • Hospital São Lucas Sergipe - Rede D´or São LuizRecruiting
  • Hospital Dr. Léo Orsi Bernadres - HLOBRecruiting
  • Hospital Naval Marcílio DiasRecruiting
  • Instituto Estadual do Cérebro Paulo Niemeyer (Pró Saúde- Associação Beneficente de Assistência Social e Hospitalar)Recruiting
  • Hospital A.C Camargo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

7-day adequate antibiotic therapy

14-day adequate antibiotic therapy

Arm Description

Adequate antibiotic therapy is defined as antimicrobial treatment with at least one agent with in vitro susceptibility.

Adequate antibiotic therapy is defined as antimicrobial treatment with at least one agent with in vitro susceptibility.

Outcomes

Primary Outcome Measures

Clinical failure
Incidence of clinical failure. Clinical failure is a composite outcome defined by the presence of one of the following: Infection relapse (infection anywhere in the body by the same MDR-GNB) or Death

Secondary Outcome Measures

Days alive and free from hospitalization
Number of days in which patients are alive and out of the hospital
Days alive and free from any antibiotic therapy
Number of days in which patients are alive and free from any antibiotic therapy
Occurrence of infections caused by other MRD-GNB or other bacteria
Incidence of infections caused by other MRD-GNB or other bacteria
Length of intensive care unit stay
Number of days in which patients stayed at intensive care unit
Acute kidney injury
Incidence of acute kidney injury, according to Kidney Disease: Improving Global Outcomes (KDIGO) criteria
Diarrhea for any cause
Incidence of any diarrhea. Diarrhea is defined as 3 or more episodes per day.
Confirmed infection by Clostridioides difficile
Incidence of Clostridioides difficile infection
Hemodynamic instability lasting more than 6 hours
Incidence of hemodynamic instability lasting more than 6 hours. Hemodynamic instability is defined as hypotension that requires the use of doses of dopamine above 15 mcg/kg/min, epinephrine above 0.1 mcg/kg/min, or norepinephrine above 0.1 mcg/kg/min
Other adverse events related to antimicrobial therapy
Incidence of any other adverse event related to antimicrobial therapy

Full Information

First Posted
December 31, 2021
Last Updated
September 11, 2023
Sponsor
Hospital Moinhos de Vento
search

1. Study Identification

Unique Protocol Identification Number
NCT05210387
Brief Title
Seven Versus 14 Days of Antibiotic Therapy for Multidrug-resistant Gram-negative Bacilli Infections
Acronym
OPTIMISE
Official Title
Open-label, Randomized Clinical Trial to Assess the Non-inferiority of 7-day Antibiotic Therapy Compared to Conventional 14-day Treatment in Multidrug-resistant Gram-negative Bacilli Infections
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 27, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Moinhos de Vento

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Antimicrobial resistance is a major global problem, particularly in hospital-acquired infections (HAIs). Gram-negative bacilli (GNB), including Enterobacterales, Pseudomonas aeruginosa, and Acinetobacter baumannii, are among the most common pathogens associated with multidrug resistance and HAIs. These bacteria are of special concern because few therapeutic options are available. Traditionally, the duration of treatment for severe multidrug-resistant (MDR)-GNB infections is 14 days. Studies of severe infections by GNB, regardless of susceptibility profile, have shown that shorter antimicrobial treatments are not inferior to traditional durations of therapy and are associated with a lower incidence of adverse effects. However, there are currently no studies assessing whether shorter duration of antimicrobial treatment is effective for MDR-GNB. This open-label, randomized clinical trial aims to assess the non-inferiority of 7-day antibiotic therapy compared to conventional 14-day treatment in severe infections by MDR-GNB.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carbapenem-Resistant Enterobacteriaceae Infection, Bloodstream Infection, Severe Infection, Pseudomonas Aeruginosa, Acinetobacter Infections, Gram-Negative Bacterial Infections, Human, Carbapenem Resistant Bacterial Infection, Bacteremia, Sepsis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
520 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
7-day adequate antibiotic therapy
Arm Type
Experimental
Arm Description
Adequate antibiotic therapy is defined as antimicrobial treatment with at least one agent with in vitro susceptibility.
Arm Title
14-day adequate antibiotic therapy
Arm Type
Active Comparator
Arm Description
Adequate antibiotic therapy is defined as antimicrobial treatment with at least one agent with in vitro susceptibility.
Intervention Type
Other
Intervention Name(s)
Duration of therapy
Intervention Description
In experimental group patients with severe infection caused by MDR-GNB and who present a clinical response on day 7 (±1) of adequate antimicrobial therapy, the therapy will be suspended. The active control group will continue therapy until day 14 (±1).
Primary Outcome Measure Information:
Title
Clinical failure
Description
Incidence of clinical failure. Clinical failure is a composite outcome defined by the presence of one of the following: Infection relapse (infection anywhere in the body by the same MDR-GNB) or Death
Time Frame
28 days after randomization
Secondary Outcome Measure Information:
Title
Days alive and free from hospitalization
Description
Number of days in which patients are alive and out of the hospital
Time Frame
28 days after randomization
Title
Days alive and free from any antibiotic therapy
Description
Number of days in which patients are alive and free from any antibiotic therapy
Time Frame
28 days after randomization
Title
Occurrence of infections caused by other MRD-GNB or other bacteria
Description
Incidence of infections caused by other MRD-GNB or other bacteria
Time Frame
28 days after randomization
Title
Length of intensive care unit stay
Description
Number of days in which patients stayed at intensive care unit
Time Frame
28 days after randomization
Title
Acute kidney injury
Description
Incidence of acute kidney injury, according to Kidney Disease: Improving Global Outcomes (KDIGO) criteria
Time Frame
28 days after randomization
Title
Diarrhea for any cause
Description
Incidence of any diarrhea. Diarrhea is defined as 3 or more episodes per day.
Time Frame
28 days after randomization
Title
Confirmed infection by Clostridioides difficile
Description
Incidence of Clostridioides difficile infection
Time Frame
28 days after randomization
Title
Hemodynamic instability lasting more than 6 hours
Description
Incidence of hemodynamic instability lasting more than 6 hours. Hemodynamic instability is defined as hypotension that requires the use of doses of dopamine above 15 mcg/kg/min, epinephrine above 0.1 mcg/kg/min, or norepinephrine above 0.1 mcg/kg/min
Time Frame
14 days after randomization
Title
Other adverse events related to antimicrobial therapy
Description
Incidence of any other adverse event related to antimicrobial therapy
Time Frame
28 days after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Infection's diagnosis while in the ICU Severe infection in any site (defined as the presence of sepsis/septic shock or bloodstream infection or pneumonia) associated with a positive culture by MRD-GNB (Acinetobacter baumannii complex, Pseudomonas aeruginosa, and Enterobacterales bacteria, only susceptible to carbapenems and/or polymyxins) Hemodynamically stable and afebrile (axillary temperature less than 37.8ºC) for at least 48 hours on day 7 of adequate antibiotic therapy Consent of the team providing care to the patient regarding their inclusion in the research Exclusion criteria Inclusion in other experimental studies involving antimicrobial therapy Infections that have as the primary site: endocarditis/endovascular infection, necrotizing fasciitis, osteomyelitis, abdominal abscess or other abdominal infections requiring surgical intervention (except infections that have been treated surgically, with curative character within the first 3 days of appropriate antimicrobial therapy), central nervous system Infections, empyema, prosthetic infection; Immunosuppression defined as: neutrophil cells <1000/mm³ in the current hospitalization, HIV/AIDS diagnosis with last CD4 count <200/mm³, solid organ transplantation in the last year and/or need for increased immunosuppression due to acute rejection in the last year, hematopoietic stem cell transplantation in the last year, and/or current therapy for chronic graft-versus-host disease Positive blood cultures for the same pathogen within 48 hours prior to randomization, when collected Uncontrolled concomitant infection with another GNB (regardless of susceptibility profile) Previous inclusion in this study Known pregnancy Patient in palliative care who has already decided not to restart antimicrobials, if necessary, or hemodynamic support measures.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alexandre Prehn Zavascki
Phone
+55 51 99714-9578
Email
alexandre.zavascki@hmv.org.br
First Name & Middle Initial & Last Name or Official Title & Degree
Beatriz Arns
Phone
+55 51 98034-0635
Email
beatriz.arns@hmv.org.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandre Prehn Zavascki
Organizational Affiliation
Hospital Moinhos de Vento
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Cleriston de Andrade
City
Feira De Santana
State/Province
Bahia
ZIP/Postal Code
44089-340
Country
Brazil
Individual Site Status
Suspended
Facility Name
Hospital Couto Maia
City
Salvador
State/Province
Bahia
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Verônica Diniz Rocha
Facility Name
Hospital da Cidade
City
Salvador
State/Province
Bahia
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
André Luiz Nunes Gobatto
Facility Name
Hospital OTO clinica
City
Fortaleza
State/Province
Ceará
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fábio Holanda Lacerda
Facility Name
Instituto Hospital de Base do Distrito Federal
City
Brasília
State/Province
Distrito Federal
ZIP/Postal Code
70330-150
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Glécia Carla Rocha
Phone
+55 61 998815345
Email
gleciacarla@yahoo.com.br
Facility Name
Hospital Universitário de Brasília
City
Brasília
State/Province
Distrito Federal
ZIP/Postal Code
70840-901
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Valéria Paes Lima
Phone
+55 61 999160311
Email
valeriapaes@yahoo.com.br
Facility Name
Hospital Evangélico de Vila Velha
City
Vila Velha
State/Province
Espirito Santo
ZIP/Postal Code
29118-060
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Livia Medeiros Almeida Dutra
Phone
+55 27 99932-7799
Email
livia_almeida_@hotmail.com
Facility Name
Hospital Presidente Vargas
City
São Luís
State/Province
Maranhão
ZIP/Postal Code
65040-450
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kairo Daniel Nunes de Oliveira Cardozo
Facility Name
Santa Casa de Misericórdia de Belo Horizonte
City
Belo Horizonte
State/Province
Minas Gerais
ZIP/Postal Code
30150-221
Country
Brazil
Individual Site Status
Suspended
Facility Name
Hospital Vila da Serra (Instituto Materno Infantil de Minas Gerais S/A)
City
Nova Lima
State/Province
Minas Gerais
ZIP/Postal Code
34000-000
Country
Brazil
Individual Site Status
Suspended
Facility Name
Irmandade da Santa Casa de Misericórdia de Passos
City
Passos
State/Province
Minas Gerais
ZIP/Postal Code
37904-020
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vanildes de Fátima Fernandes Silva
Phone
+55 35 99707-3145
Email
vanfern@yahoo.com.br
Facility Name
Hospital Universitário da Universidade Estadual de Londrina
City
Londrina
State/Province
Paraná
ZIP/Postal Code
86038-350
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cláudia Maria Dantas de Maio Carrilho
Phone
+55 43 999941560
Email
maiocarrilho@gmail.com
Facility Name
Hospital Municipal de Maringá
City
Maringá
State/Province
Paraná
ZIP/Postal Code
87053-270
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francielle Constantino Pereira
Phone
+55 44 988032383
Email
francielle90@hotmail.com
Facility Name
Hospital Regional Baixo Amazonas
City
Santarém
State/Province
Pará
Country
Brazil
Individual Site Status
Suspended
Facility Name
Hospital do Tricentenário
City
Olinda
State/Province
Pernambuco
ZIP/Postal Code
53120-420
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carlos Sérgio Luna Gomes Duarte
Phone
+55 81 98818-2280
Email
duartecslg@hotmail.com
Facility Name
Hospital São João Batista
City
Volta Redonda
State/Province
Rio De Janeiro
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Graciele Medeiros
Facility Name
Hospital Tacchini
City
Bento Gonçalves
State/Province
Rio Grande Do Sul
ZIP/Postal Code
95700-068
Country
Brazil
Individual Site Status
Suspended
Facility Name
Hospital Geral Caxias do Sul
City
Caxias Do Sul
State/Province
Rio Grande Do Sul
ZIP/Postal Code
95070-561
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emerson Boschi da Silva
Phone
+55 54 99968-0563
Email
boschimd@gmail.com
Facility Name
Hospital de Clinicas de Porto Alegre
City
Porto Alegre
State/Province
Rio Grande Do Sul
ZIP/Postal Code
90035-903
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thiago Costa Lisboa
Phone
+55 51 997826832
Email
tlisboa@hotmail.com
Facility Name
Hospital Ernesto Dornelles
City
Porto Alegre
State/Province
Rio Grande Do Sul
ZIP/Postal Code
90160-092
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carla Bittencourt Rynkowski
Phone
+55 51 997525225
Email
carla.rynkowski@hed.com.br
Facility Name
Hospital Nossa Senhora da Conceição
City
Porto Alegre
State/Province
Rio Grande Do Sul
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guilherme Geraldo Lovato Sório
Facility Name
Hospital São Lucas da PUC
City
Porto Alegre
State/Province
Rio Grande Do Sul
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Diego Rodrigues Falci
Facility Name
Hospital Santa Cruz
City
Santa Cruz Do Sul
State/Province
Rio Grande Do Sul
ZIP/Postal Code
96810-072
Country
Brazil
Individual Site Status
Suspended
Facility Name
Hospital Ana Nery
City
Santa Cruz Do Sul
State/Province
Rio Grande Do Sul
ZIP/Postal Code
96835-090
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rodrigo Morel Vieira de Melo
Phone
+55 71 99162-2000
Email
vieirademelorm@gmail.com
Facility Name
Hospital São Lucas Sergipe - Rede D´or São Luiz
City
Aracaju
State/Province
Sergipe
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roberta Machado de Souza
Facility Name
Hospital Dr. Léo Orsi Bernadres - HLOB
City
Itapetininga
State/Province
São Paulo
ZIP/Postal Code
18.030-070
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vivian Menezes Irineu
Facility Name
Hospital Naval Marcílio Dias
City
Rio De Janeiro
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vicente Vaz
Facility Name
Instituto Estadual do Cérebro Paulo Niemeyer (Pró Saúde- Associação Beneficente de Assistência Social e Hospitalar)
City
Rio De Janeiro
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pedro Martins Pereira Kurtz
Phone
+55 21 98330-8338
Email
kurtzpedro@mac.com
Facility Name
Hospital A.C Camargo
City
São Paulo
Country
Brazil
Individual Site Status
Suspended

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Seven Versus 14 Days of Antibiotic Therapy for Multidrug-resistant Gram-negative Bacilli Infections

We'll reach out to this number within 24 hrs