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Purpose of the trial: Evaluate the efficacy and safety of the device of self-invention of continuous oropharyngeal aspiration denominated "SUPRAtube" in patients with orotracheal intubation and mechanical ventilation.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Supratube | Other | Patient with orotracheal intubation and supratube device |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Supratube | Device | Aspiration of orotracheal secretions with supratube device |
| |
| Measure | Description | Time Frame |
|---|---|---|
| aspirated secretions | volume of aspirated secretions | 24 hours after intubation |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | Adverse events related to supratube device use | 24 hours after intubation |
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Inclusion Criteria:
• Endotracheal intubation and invasive mechanical ventilation,
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Fundación Cardiovascular de Colombia | Piedecuesta | Santander Department | 681011 | Colombia |
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| ID | Term |
|---|---|
| D011015 | Pneumonia, Aspiration |
| ID | Term |
|---|---|
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
| D008171 | Lung Diseases |
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| Reference |
| Other |
Usual aspiration with any other device |
|
| D012140 |
| Respiratory Tract Diseases |