Addition of Tobramycin Inhalation in the Treatment of Ventilator Associated Pneumonia (VAPORISE)
Primary Purpose
Ventilator Associated Pneumonia (VAP)
Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
tobramycin inhalation
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Ventilator Associated Pneumonia (VAP)
Eligibility Criteria
Inclusion Criteria:
- Mechanical ventilation 48 hours or more
- New or progressive radiologic pulmonary infiltrate
Together with at least two of the following three criteria (< 24 h):
- temperature >38°C
- leukocytosis >12,000/mm3 or leucopenia <4,000/mm3
- purulent respiratory secretions
Exclusion Criteria:
- patients with allergy to tobramycin
- pregnancy
- expected to die within 72 hours after enrollment
Sites / Locations
- Erasmus MC
- Hospital Clinic
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
tobramycin inhalation
Placebo
Arm Description
twice daily tobramycin inhalation (Bramitob) 300 mg and standard intravenous antibiotics treatment
twice daily placebo inhalation and standard intravenous antibiotics treatment
Outcomes
Primary Outcome Measures
response after 72 h of treatment
non response is considered when at least one of the following is present
No improvement of the arterial O2 tension to inspired O2 fraction ratio
Persistence of fever (≥38°C) or hypothermia (<35.5°C) together with purulent respiratory secretions
increase in the pulmonary infiltrates on chest radiograph of greater than or equal to 50%
occurrence of septic shock or multiple organ dysfunction syndrome, defined as three or more organ system failures not present on Day 1
Secondary Outcome Measures
Mortality rate
30-day and 90- day mortality rate
Mortality rate
30-day and 90- day mortality rate
ICU survival
Absence of hospital admittance at day 60
Discharge from the ICU
Patients will be followed during ICU stay and evaluated at discharge from ICU, expected average time of discharge is 10 days
Ventilator free days at day 28
Adverse events
Adverse events
Adverse events
Adverse events
Adverse events
Adverse events
Day of normalisation of CRP
Day of normalisation of CRP
Day of normalisation of CRP
Day of normalisation of CRP
Day of normalisation of CRP
Day of normalisation of CRP
Eradication of pathogens
Eradication of pathogens
Eradication of pathogens
Eradication of pathogens
Eradication of pathogens
Clinical Pulmonary Infectious Score (CPIS)
Clinical Pulmonary Infectious Score (CPIS)
Clinical Pulmonary Infectious Score (CPIS)
Clinical Pulmonary Infectious Score (CPIS)
Clinical Pulmonary Infectious Score (CPIS)
APACHE II score
APACHE II score
APACHE II score
APACHE II score
APACHE II score
Multiple Organ Dysfunction score (MODS)
Multiple Organ Dysfunction score (MODS)
Multiple Organ Dysfunction score (MODS)
Multiple Organ Dysfunction score (MODS)
Multiple Organ Dysfunction score (MODS)
Sequential Organ Failure Assessment score (SOFA)
Sequential Organ Failure Assessment score (SOFA)
Sequential Organ Failure Assessment score (SOFA)
Sequential Organ Failure Assessment score (SOFA)
Sequential Organ Failure Assessment score (SOFA)
Lung Injury Score (LIS)
Lung Injury Score (LIS)
Lung Injury Score (LIS)
Lung Injury Score (LIS)
Lung Injury Score (LIS)
Day of normalisation of procalcitonin (PCT)
Day of normalisation of procalcitonin (PCT)
Day of normalisation of procalcitonin (PCT)
Day of normalisation of procalcitonin (PCT)
Day of normalisation of procalcitonin (PCT)
Day of normalisation of procalcitonin (PCT)
Day of normalisation of chest X-ray
Day of normalisation of chest X-ray
Day of normalisation of chest X-ray
Day of normalisation of chest X-ray
Day of normalisation of chest X-ray
Day of normalisation of chest X-ray
Full Information
NCT ID
NCT02440828
First Posted
March 13, 2015
Last Updated
August 17, 2021
Sponsor
Erasmus Medical Center
Collaborators
Chiesi Farmaceutici S.p.A.
1. Study Identification
Unique Protocol Identification Number
NCT02440828
Brief Title
Addition of Tobramycin Inhalation in the Treatment of Ventilator Associated Pneumonia
Acronym
VAPORISE
Official Title
Ventilator Associated Pneumonia: Addition of Tobramycin Inhalation Antibiotic Treatment to Standard IV Antibiotic Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
March 1, 2020 (Actual)
Study Completion Date
July 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Erasmus Medical Center
Collaborators
Chiesi Farmaceutici S.p.A.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study evaluates the addition of tobramycin inhalation treatment to standard intravenous therapy in the treatment of ventilator associated pneumonia.
Detailed Description
Rationale: Approximately 9-27% of mechanically ventilated patients in the intensive care unit (ICU) develop ventilator-associated pneumonia (VAP). Patients in whom VAP develops have a higher mortality rate up to 50%, stay longer in the intensive care unit (ICU), and require more resources than those without the disease. Despite the availability of modern ICU care and modern antibiotics, the overall clinical cure rate after 72 hours of antibiotic treatment for VAP is only 40%. The cure rate for Pseudomonas aeruginosa is even lower. It is unclear why VAP cure rates are so low. The ATS guidelines recommend IV antibiotic treatment (IV AB), especially directed against gram-negative microorganisms. However, the relatively poor response rates seen with intravenous therapy of VAP and the emergence of MDR organisms makes new treatment options desirable. The ATS/IDSA VAP guidelines recommend that "adjunctive therapy with an inhaled aminoglycoside or polymyxin (colistin) for MDR Gram-negative pneumonia should be considered, especially in patients who are not improving". It is therefore necessary to investigate whether adjunctive therapy with inhalation Tobramycin could ameliorate prognosis. The recommendations by the Society of Infectious Diseases Pharmacists are similar.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventilator Associated Pneumonia (VAP)
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
tobramycin inhalation
Arm Type
Experimental
Arm Description
twice daily tobramycin inhalation (Bramitob) 300 mg and standard intravenous antibiotics treatment
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
twice daily placebo inhalation and standard intravenous antibiotics treatment
Intervention Type
Drug
Intervention Name(s)
tobramycin inhalation
Other Intervention Name(s)
Bramitob
Intervention Description
tobramycin inhalation 300 mg twice daily
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
NaCl 0.9% inhalation 4 ml
Intervention Description
NaCl 0.9% inhalation 4 ml twice daily
Primary Outcome Measure Information:
Title
response after 72 h of treatment
Description
non response is considered when at least one of the following is present
No improvement of the arterial O2 tension to inspired O2 fraction ratio
Persistence of fever (≥38°C) or hypothermia (<35.5°C) together with purulent respiratory secretions
increase in the pulmonary infiltrates on chest radiograph of greater than or equal to 50%
occurrence of septic shock or multiple organ dysfunction syndrome, defined as three or more organ system failures not present on Day 1
Time Frame
72 hours
Secondary Outcome Measure Information:
Title
Mortality rate
Description
30-day and 90- day mortality rate
Time Frame
day 30
Title
Mortality rate
Description
30-day and 90- day mortality rate
Time Frame
day 90
Title
ICU survival
Time Frame
day 90
Title
Absence of hospital admittance at day 60
Time Frame
day 60
Title
Discharge from the ICU
Description
Patients will be followed during ICU stay and evaluated at discharge from ICU, expected average time of discharge is 10 days
Time Frame
up to 60 days
Title
Ventilator free days at day 28
Time Frame
up to 28 days
Title
Adverse events
Time Frame
day 1
Title
Adverse events
Time Frame
day 4
Title
Adverse events
Time Frame
day 8
Title
Adverse events
Time Frame
day 14
Title
Adverse events
Time Frame
day 30
Title
Adverse events
Time Frame
day 90
Title
Day of normalisation of CRP
Time Frame
day 1
Title
Day of normalisation of CRP
Time Frame
day 4
Title
Day of normalisation of CRP
Time Frame
day 8
Title
Day of normalisation of CRP
Time Frame
day 14
Title
Day of normalisation of CRP
Time Frame
day 30
Title
Day of normalisation of CRP
Time Frame
day 90
Title
Eradication of pathogens
Time Frame
day 4
Title
Eradication of pathogens
Time Frame
day 8
Title
Eradication of pathogens
Time Frame
day 14
Title
Eradication of pathogens
Time Frame
day 30
Title
Eradication of pathogens
Time Frame
day 90
Title
Clinical Pulmonary Infectious Score (CPIS)
Time Frame
Day 1
Title
Clinical Pulmonary Infectious Score (CPIS)
Time Frame
Day 4
Title
Clinical Pulmonary Infectious Score (CPIS)
Time Frame
Day 8
Title
Clinical Pulmonary Infectious Score (CPIS)
Time Frame
Day 14
Title
Clinical Pulmonary Infectious Score (CPIS)
Time Frame
discharge ICU, expected average time of discharge is 10 days
Title
APACHE II score
Time Frame
Day 1
Title
APACHE II score
Time Frame
Day 4
Title
APACHE II score
Time Frame
Day 8
Title
APACHE II score
Time Frame
Day 14
Title
APACHE II score
Time Frame
discharge ICU, expected average time of discharge is 10 days
Title
Multiple Organ Dysfunction score (MODS)
Time Frame
Day 1
Title
Multiple Organ Dysfunction score (MODS)
Time Frame
Day 4
Title
Multiple Organ Dysfunction score (MODS)
Time Frame
Day 8
Title
Multiple Organ Dysfunction score (MODS)
Time Frame
Day 14
Title
Multiple Organ Dysfunction score (MODS)
Time Frame
discharge ICU, expected average time of discharge is 10 days
Title
Sequential Organ Failure Assessment score (SOFA)
Time Frame
Day 1
Title
Sequential Organ Failure Assessment score (SOFA)
Time Frame
Day 4
Title
Sequential Organ Failure Assessment score (SOFA)
Time Frame
Day 8
Title
Sequential Organ Failure Assessment score (SOFA)
Time Frame
Day 14
Title
Sequential Organ Failure Assessment score (SOFA)
Time Frame
discharge ICU, expected average time of discharge is 10 days
Title
Lung Injury Score (LIS)
Time Frame
Day 1
Title
Lung Injury Score (LIS)
Time Frame
Day 4
Title
Lung Injury Score (LIS)
Time Frame
Day 8
Title
Lung Injury Score (LIS)
Time Frame
Day 14
Title
Lung Injury Score (LIS)
Time Frame
discharge ICU, expected average time of discharge is 10 days
Title
Day of normalisation of procalcitonin (PCT)
Time Frame
day 1
Title
Day of normalisation of procalcitonin (PCT)
Time Frame
day 4
Title
Day of normalisation of procalcitonin (PCT)
Time Frame
day 8
Title
Day of normalisation of procalcitonin (PCT)
Time Frame
day 14
Title
Day of normalisation of procalcitonin (PCT)
Time Frame
day 30
Title
Day of normalisation of procalcitonin (PCT)
Time Frame
day 90
Title
Day of normalisation of chest X-ray
Time Frame
day 1
Title
Day of normalisation of chest X-ray
Time Frame
day 4
Title
Day of normalisation of chest X-ray
Time Frame
day 8
Title
Day of normalisation of chest X-ray
Time Frame
day 14
Title
Day of normalisation of chest X-ray
Time Frame
day 30
Title
Day of normalisation of chest X-ray
Time Frame
day 90
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Mechanical ventilation 48 hours or more
New or progressive radiologic pulmonary infiltrate
Together with at least two of the following three criteria (< 24 h):
temperature >38°C
leukocytosis >12,000/mm3 or leucopenia <4,000/mm3
purulent respiratory secretions
Exclusion Criteria:
patients with allergy to tobramycin
pregnancy
expected to die within 72 hours after enrollment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Menno Van der Eerden, MD, PhD
Organizational Affiliation
Erasmus Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Erasmus MC
City
Rotterdam
ZIP/Postal Code
3000CA
Country
Netherlands
Facility Name
Hospital Clinic
City
Barcelona
ZIP/Postal Code
08036
Country
Spain
12. IPD Sharing Statement
Learn more about this trial
Addition of Tobramycin Inhalation in the Treatment of Ventilator Associated Pneumonia
We'll reach out to this number within 24 hrs