A clinical study for safety and efficacy of a device automatically remove saliva and other fluid and other secretions from the airway ans also does mouthwash for the intubated patients.
- Conditions
- Health Condition 1: null- Orotracheally intubated patients on the ventilator.
- Registration Number
- CTRI/2018/04/013291
- Lead Sponsor
- Coeo Labs private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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.
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method