Comparison of high flow nasal cannula and non invasive ventilation in transport of critically ill patients in hospital
Not Applicable
- Conditions
- Health Condition 1: J00-J99- Diseases of the respiratory system
- Registration Number
- CTRI/2023/07/054931
- Lead Sponsor
- Eras Lucknow Medical College and Hospital Lucknow
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Age 18 years or above
2) Critically ill patients requiring intra- hospital transport
Exclusion Criteria
1) Severe respiratory failure requiring immediate tracheal intubation (respiratory frequency 40 times/min, severe hypoxia, severe respiratory acidosis with a ph <7.25, glasgow score <8).
2) A contraindication to NIV (oral and facial trauma, excessive phlegm with poor expectoration ability, hemodynamic instability).
3) Patients with poor short term prognosis (very high risk of death within seven days or receiving palliative care).
4) Pregnant women.
5) Carriers of an implantable defibrillator or pacemaker.
6) Tracheostomized patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) To determine the effect on oxygenation, by measuring SpO2 <br/ ><br>during transportation. <br/ ><br> <br/ ><br>2) To determine the need to escalate/de-escalate respiratory <br/ ><br>support/ invasive mechanical ventilation after ICU admission. <br/ ><br>Timepoint: 1) during tansportation of patient <br/ ><br>2) 5 minutes, 15 minutes, 1 hour, 24 hours, 48 hours after transport. <br/ ><br>
- Secondary Outcome Measures
Name Time Method to record: <br/ ><br>1.duration of respiratory support. <br/ ><br>2.adverse events during transportation. <br/ ><br>3.length of icu stay. <br/ ><br>4.length of hospital stay. <br/ ><br>5.icu mortality. <br/ ><br>6.hospital mortality.Timepoint: 72 hours after transport, 7 days after transport