Polymyxin B Monotherapy vs Combination Therapy in Critically Ill Patients With Multi-drug Resistant Pathogens (MUSEUM)
Primary Purpose
Trauma, Resistant Infection, Critical Illness
Status
Unknown status
Phase
Phase 3
Locations
Puerto Rico
Study Type
Interventional
Intervention
Polymyxin B
Sponsored by
About this trial
This is an interventional treatment trial for Trauma focused on measuring Acinetobacter, Polymyxins, Imipenem, Pseudomona, Klebsiella
Eligibility Criteria
Inclusion Criteria:
- 21 years or older admitted to the Intensive Care Unit of the Puerto Rico Trauma Hospital ° Consent form signed,
- Clinical and microbiological evidence of a MDR infection related to HAP, VAP, cUTI or BSI.
- The pathogen should be resistant to almost all antibiotics, AND/OR intermediate resistant to some of the antibiotics, AND/OR susceptible only to a class of antibiotic (i.e. aminoglycosides which are NOT recommended as monotherapy), AND/OR the clinician decision is to start the patient on polymyxin B due to severity of the infection.
- Patient with a diagnosis of MDR infection, who have not received antibiotics at all; OR if received would be < 72 hours with polymyxin B or imipenem at/or after the diagnosis of MDR AND/OR at the time of randomization
- Have a life expectancy of > 24 hours according to the attending physician's criteria.
Exclusion Criteria:
- Pregnant woman
- Prisoners
- Severe hepatic failure (defined by serum conjugated bilirubin > 3 mg/dL)
- End-stage renal disease requiring hemodialysis
- Hypersensitivity to any study drug
- Septic shock at the moment of randomization
- Died within 48 hours of starting the study
Sites / Locations
- Trauma HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Experimental
Arm Label
Polymyxin B monotherapy
Polymyxin B plus Carbapenem
Arm Description
Intravenous piggyback with Polymyxin B and control(Normal saline)
Intravenous piggyback with Polymyxin B plus Carbapenem
Outcomes
Primary Outcome Measures
Resolution of the evidence of clinical infection
Resolution of infection will be subjective to clinical criteria of the physician, AND patient has to be afebrile (temperature < 38°C), or normothermic (temperature 36-37.5°C), AND have white blood cell count within normal limits (> 4,000 and < 10,000 cells/mm3).
Secondary Outcome Measures
30-day mortality
Thirty-day (30-day) mortality will be measured from the day of hospital admission until discharge.
Recurrence of infection
The recurrence of infection will be defined as a new superinfection by the same or other species than the initial infection that is multidrug-resistant.
Length of stay at Hospital
Will be measured from the day of hospital admission until discharge.
Length of stay at ICU.
Will be measured from the day of ICU admission until transfer or discharge.
Full Information
NCT ID
NCT03159078
First Posted
May 10, 2017
Last Updated
February 7, 2019
Sponsor
University of Puerto Rico
1. Study Identification
Unique Protocol Identification Number
NCT03159078
Brief Title
Polymyxin B Monotherapy vs Combination Therapy in Critically Ill Patients With Multi-drug Resistant Pathogens
Acronym
MUSEUM
Official Title
Polymyxin B Monotherapy Versus Polymyxin B-Carbapenem Combination Therapy in Critically Ill Patients With Multi-drug Resistant Gram-negative Infection: A Prospective, Parallel-Group, Double-Blind, Randomized Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 25, 2017 (Actual)
Primary Completion Date
December 1, 2019 (Anticipated)
Study Completion Date
December 1, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Puerto Rico
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to assess the safety and efficacy of polymyxin B as monotherapy versus a combined polymyxin B-carbapenem therapy against multidrug-resistant (MDR) gram negative infections. The investigators intend to evaluate if this synergistic drug regimen correlates with improved outcomes against gram-negative infections in critically ill patients including: better clinical resolution, reduced length of stay at hospital, reduced length of stay at the intensive care unit, and less recurrence of infection.
Detailed Description
The "MUSEUM" trial is a single-center, prospective, parallel-group, double-blind, randomized, controlled study design. The trial will be conducted at the Intensive Care Unit of the Puerto Rico Trauma Hospital located in San Juan, Puerto Rico. Patients with clinical and microbiological evidence of an Multi-drug resistant infection related to Hospital-acquired pneumonia (HAP), Ventilator-associated pneumonia (VAP), Complicated Urinary tract infection (cUTI) or Bloodstream infection (BSI) will be considered candidates for the study. The pathogen should be resistant to all antibiotics except to polymyxin B. With a predicted survival rate of 67% (hazard ratio of 0.33), a significance of α = 0.05, power of 80%, and assuming a dropout rate of 15%, the estimated sample size is n = 40 patients (20 per group). In terms of safety, the most clinically relevant adverse effects are nephrotoxicity and neurotoxicity, which will be evaluated and adjudicated. The recurrence of infection will be defined as a new superinfection by the same or other species than the initial infection that is multidrug-resistant. Length of stay at the Hospital will be measured from the day of admission until the day of discharge. Length of stay in the ICU will be measured from the day of admission until the day of discharge from the unit. To our knowledge, this will be the first prospective, double blind, randomized, controlled clinical trial in representation of the critically ill trauma patients infected with Multi-drug resistant pathogens.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trauma, Resistant Infection, Critical Illness
Keywords
Acinetobacter, Polymyxins, Imipenem, Pseudomona, Klebsiella
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
One arm with Polyxyxin B monotherapy and another arm with Polymyxin B plus carbapenem
Masking
ParticipantCare ProviderInvestigator
Masking Description
Double blind, Double dummy
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Polymyxin B monotherapy
Arm Type
Other
Arm Description
Intravenous piggyback with Polymyxin B and control(Normal saline)
Arm Title
Polymyxin B plus Carbapenem
Arm Type
Experimental
Arm Description
Intravenous piggyback with Polymyxin B plus Carbapenem
Intervention Type
Drug
Intervention Name(s)
Polymyxin B
Other Intervention Name(s)
Imipenem, (Primaxin)
Intervention Description
Comparison of Poly B monotherapy vs Polymyxin B plus carbapenem in MDR infections
Primary Outcome Measure Information:
Title
Resolution of the evidence of clinical infection
Description
Resolution of infection will be subjective to clinical criteria of the physician, AND patient has to be afebrile (temperature < 38°C), or normothermic (temperature 36-37.5°C), AND have white blood cell count within normal limits (> 4,000 and < 10,000 cells/mm3).
Time Frame
7-14 days, according to site of infection
Secondary Outcome Measure Information:
Title
30-day mortality
Description
Thirty-day (30-day) mortality will be measured from the day of hospital admission until discharge.
Time Frame
30 days
Title
Recurrence of infection
Description
The recurrence of infection will be defined as a new superinfection by the same or other species than the initial infection that is multidrug-resistant.
Time Frame
30 days
Title
Length of stay at Hospital
Description
Will be measured from the day of hospital admission until discharge.
Time Frame
30 days
Title
Length of stay at ICU.
Description
Will be measured from the day of ICU admission until transfer or discharge.
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
21 years or older admitted to the Intensive Care Unit of the Puerto Rico Trauma Hospital ° Consent form signed,
Clinical and microbiological evidence of a MDR infection related to HAP, VAP, cUTI or BSI.
The pathogen should be resistant to almost all antibiotics, AND/OR intermediate resistant to some of the antibiotics, AND/OR susceptible only to a class of antibiotic (i.e. aminoglycosides which are NOT recommended as monotherapy), AND/OR the clinician decision is to start the patient on polymyxin B due to severity of the infection.
Patient with a diagnosis of MDR infection, who have not received antibiotics at all; OR if received would be < 72 hours with polymyxin B or imipenem at/or after the diagnosis of MDR AND/OR at the time of randomization
Have a life expectancy of > 24 hours according to the attending physician's criteria.
Exclusion Criteria:
Pregnant woman
Prisoners
Severe hepatic failure (defined by serum conjugated bilirubin > 3 mg/dL)
End-stage renal disease requiring hemodialysis
Hypersensitivity to any study drug
Septic shock at the moment of randomization
Died within 48 hours of starting the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juan M Maldonado Lozada, Pharm D
Phone
7875570612
Email
juan.maldonado12@upr.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Pablo Rodriguez, MD
Phone
787430-4415
Email
pablororc@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan M Maldonado Lozada, PharmD
Organizational Affiliation
School of Pharmacy, University of Puerto Rico
Official's Role
Principal Investigator
Facility Information:
Facility Name
Trauma Hospital
City
San Juan
ZIP/Postal Code
00922-2129
Country
Puerto Rico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juan M Maldonado, Pharm D
Phone
787-557-0612
Email
juan.maldonado12@upr.edu
First Name & Middle Initial & Last Name & Degree
Pablo Rodriguez, MD
Phone
787-4304415
Email
pablororc@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
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Links:
URL
http://www.cdc.gov/HAI/infectionTypes.html
Description
Type of Healthcare-Associated Infections
URL
https://www.cdc.gov/hai/organisms/gram-negative-bacteria.html
Description
Gram-negative Bacteria Infections in Healthcare Settings
URL
https://clinicaltrials.gov/ct2/show/record/nct01597973?term=nct01597973&rank=1
Description
Trial for the Treatment of Extensively Drug-Resistant Gram-negative Bacilli
URL
https://clinicaltrials.gov/ct2/show/record/nct01732250?term=nct01732250&rank=1
Description
Multicenter Open-label Randomized Controlled Trial (RCT) to Compare Colistin Alone Versus Colistin Plus Meropenem
URL
https://www.merck.com/product/usa/pi_circulars/p/primaxin/primaxin_iv_pi.pdf
Description
Primaxin I.V. (Imipenem and Cilastatin for IV Injection).
URL
https://www.aacc.org/store/books/9200/performance-standards-for-antimicrobial-susceptibility-testing.aspx
Description
Performance standards for antimicrobial susceptibility testing: twenty-six informational supplement.
Learn more about this trial
Polymyxin B Monotherapy vs Combination Therapy in Critically Ill Patients With Multi-drug Resistant Pathogens
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