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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
NameTimeMethod
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
NameTimeMethod
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
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