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unable to enroll patients adequately
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The purpose of this study is to collect data on patients who are on breathing machines (ventilators) in the Trauma Surgical Intensive Care Unit (TSICU). This data may help us to determine if one form of assisted breathing is better than another. The two forms of assisted breathing being compared in this study are called BiVent and SIMV. (7) BiVent and SIMV are both delivered by a ventilator but differ in how they assist breathing. SIMV is an older form of mechanical breathing that blows air into the lungs to inflate the lungs. BiVent is a newer form of mechanical ventilation that permits the patient to pull air into the lungs as we normally do. Both BiVent and SIMV are currently being used on a regular basis in the TSICU. The investigators hope that this study will determine if one method of assisted breathing is better than another in preventing complications associated with mechanically assisted breathing.
SOLV Hypothesis:
A prospective, randomized trial directly comparing open lung ventilation (OLV) with spontaneous breathing (SB) utilizing BiVent on the Maquet Servo-I versus synchronized intermittent mechanical ventilation (SIMV) will be conducted in the trauma-surgical intensive care unit at the University Hospital (TSICU). Both OLV-SB and SIMV protocols have been designed according to lung protective strategies. The primary goal of the SOLV trial is to see determine if the early application of open lung ventilation will less ventilator days. In addition, several secondary endpoints will be evaluated. It is not anticipated that this study will be powered to show a mortality difference.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Open Lung Ventilation | within 24 hours of arrival trauma patients with ISS >25 will be randomized to BiVent (APRV) | ||
| SIMV | within 24 hours of arrival trauma patients with ISS >25 will be randomized to either SIMV or BiVent |
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| Measure | Description | Time Frame |
|---|---|---|
| Reduction in ventilator days | 4 years |
| Measure | Description | Time Frame |
|---|---|---|
| Progression to acute lung injury/acute respiratory distress syndrome (ALI/ARDS) | 4 years |
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Inclusion Criteria:
Exclusion Criteria:
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Adult Trauma Patients with ISS>/=25
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of New Mexico Hospital | Albuquerque | New Mexico | 87131 | United States |
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| ID | Term |
|---|---|
| D014947 | Wounds and Injuries |
| D053120 | Respiratory Aspiration |
| D055371 | Acute Lung Injury |
| ID | Term |
|---|---|
| D012120 | Respiration Disorders |
| D012140 | Respiratory Tract Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| D055370 | Lung Injury |
| D008171 | Lung Diseases |