Comparision of two barrier devices for placement of tube into trachea(windpipe)in COVID19 patients
Phase 3
- Conditions
- Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere
- Registration Number
- CTRI/2020/08/027081
- Lead Sponsor
- Department of AnaesthesiaGCS Medical CollegeHospital Research CentreAhmedabad
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
COVID positive/suspected patient
No improvement in Respiratory Distress
Tachypnea (RR >30/min)
Poor oxygenation (PaO2 :FiO2 ratio <150mmhg after 2 hour high flow O2 therapy on non invasive mode ventilation
Altered sensorium / shock/convulsion
on ABG PaO2 <60 & PaCO2 >60
Age >15 and <90 yrs
Informed consent
Exclusion Criteria
COVID negative patient
Patient with mouth opening
Age <15 and >90 years of age
Patient with airway pathology(oral, pharyngeal, laryngeal carcinoma
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Our purpose of this study to know which barrier device is better for airway manipulation in COVID 19 patientsTimepoint: 8 months
- Secondary Outcome Measures
Name Time Method HEALTHCARE WORKERS WILL HAVE BETTER SAFETY Our purpose of this study to know which barrier device is better for airway manipulation in COVID 19 patientsTimepoint: 8 months