CTRI/2018/04/013291Not yet recruiting未知
Preliminary study to assess the performance of a device designed to perform automatic suctioning of oropharyngeal and subglottic secretions and perform automated oral lavage in orotracheally intubated ICU patients.
Coeo Labs private Limited0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1.Patients requiring mechanical ventilation for 48 hrs or more
- •2. Patients must be between 18 - 75 years of age (Male or Female).
- •3. Patient must have been intubated with Portex (Smiths Medical) a CASS ET Tube.
- •4. A physician is able to place the suction lumen appropriately and fix it in position
- •5. Patient or a legal representative of the patient must be able to give written consent for the study.
Exclusion Criteria
- •1. Patient intubated for more than 12 hours
- •2. Patient admitted for cardiac surgery/post cardiac surgery
- •3. Patient admitted with tracheostomy
- •4. Patient with bleeding disorders
- •5. Patient on oral anticoagulants
- •6. Patient with head, neck or facial injury
- •7. Patient is pregnant
- •8. Patient with/post cardiac arrest
- •9. Patient has pre-existing pneumonia at time of admission
- •10. Patient has COPD requiring life-long antibiotic therapy
- •11. Patient in post-lung transplant state
Investigators
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