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Severe hypoxemia following trauma may happen in many circumstances (aspiration, ventilation-associated pneumonia, lung contusion...), most of which are not exclusively associated with a direct injury to the lungs. Severe trauma and associated musculoskeletal injuries result in the acute release of Damage-Associated Molecular Patterns (DAMPs) in plasma, many of which are made of nucleic acids. DAMPs then bind leukocytes and trigger NETosis (Neutrophil Extracellular Traps), the release of nuclear material coated with proteolytic enzymes, which ultimately promotes remote lung injury and acute respiratory distress syndrome (ARDS).
Considering that many DAMPs and all NETs are made of nucleic acids, we hypothesize that dornase alfa, a commercially available recombinant desoxyribonuclease (DNAse) could reduce DAMPs and NETs-induced lung injury in severe trauma patients under mechanical ventilation in the intensive care unit (ICU).
The primary objective is to demonstrate a reduction in the incidence of moderate to severe ARDS in severe trauma patients during the first seven ICU days from 45% to 30% by providing aerosolized dornase alfa once during the first two consecutive ICU days and compared to equivalent provision of placebo (NaCl 0,9%).
The secondary objectives are to demonstrate, by using aerosolized dornase alfa compared to placebo:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Dornase alfa | Experimental | Dornase alfa (Pulmozyme®, Roche 2500U, 2,5mL) given by aerosol in the respiratory circuit (Aerogen solo®) within 6h at day 1 and 24 hours after on day 2. |
|
| Placebo | Placebo Comparator | NaCl 0,9%, given by aerosol in the respiratory circuit within 6h at day 1 and 24 hours after on day 2. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Dornase Alfa Inhalant Solution [Pulmozyme] | Drug | Dornase alfa (Pulmozyme®, Roche 2500U, 2,5mL) given by aerosol in the respiratory circuit (Aerogen solo®) within 6h at day 1 and 24 hours after on day 2. |
| Measure | Description | Time Frame |
|---|---|---|
| The primary endpoint is the incidence of moderate to severe ARDS (PaO2/FiO2 < 200, according to the Berlin definition [ARDS definition task force et al. JAMA 2015; 307(23): 2526-2533]) in severe trauma patients (Injury Severity Score > 15). | Day 0 to Day 7 |
| Measure | Description | Time Frame |
|---|---|---|
| Static lung compliance [mL/cmH2O] | Day 0 to Day 7 | |
| Duration of mechanical ventilation [hours] | Day 0 to Day 7 | |
| Length of ICU stay [hours] |
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Inclusion Criteria:
Adult (>18) patient of either sex affiliated to the National Health Service
Exclusion Criteria:
Pregnancy or breast feeding
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Julien POTTECHER, MD | Contact | +33 388127095 | julien.pottecher@chru-strasbourg.fr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital, Strasbourg, france | Recruiting | Strasbourg | 67000 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32183886 | Derived | Pottecher J, Noll E, Borel M, Audibert G, Gette S, Meyer C, Gaertner E, Legros V, Carapito R, Uring-Lambert B, Sauleau E, Land WG, Bahram S, Meyer A, Geny B, Diemunsch P. Protocol for TRAUMADORNASE: a prospective, randomized, multicentre, double-blinded, placebo-controlled clinical trial of aerosolized dornase alfa to reduce the incidence of moderate-to-severe hypoxaemia in ventilated trauma patients. Trials. 2020 Mar 18;21(1):274. doi: 10.1186/s13063-020-4141-6. |
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| ID | Term |
|---|---|
| D009104 | Multiple Trauma |
| D012128 | Respiratory Distress Syndrome |
| D014947 | Wounds and Injuries |
| ID | Term |
|---|---|
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D012120 | Respiration Disorders |
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| ID | Term |
|---|---|
| C568813 | dornase alfa |
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| Placebos | Drug | NaCl 0,9%, given by aerosol in the respiratory circuit within 6h at day 1 and 24 hours after on day 2. |
|
| Day 0 to Day 7 |
| Length of stay in the hospital [days] | Day 0 to Day 7 |
| Incidence of multi-organ failure | according SOFA (Sepsis-related Organ Failure Assessment) to quantify organ dysfunction | Day 0 to Day 7 |
| Incidence of Ventilator-Associated Pneumonia (VAP) | Day 0 to Day 7 |
| Mortality on day 28 | Day 28 |