Evaluation of the effectiveness of high flow oxygen delivery through the nasal cannula in comparison with non-invasive ventilation in patients with COVID-19

Not Applicable

• Conditions: COVID-19.; Coronavirus infection, unspecified; B34.2

• Registration Number: IRCT20160516027929N8
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 April 2021

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Arterial blood oxygen saturation less than 90%
Signing a written consent to participate in the study
Age over 18 years

Exclusion Criteria

Pulmonary insufficiency
Acute or chronic renal failure
Pregnancy or breastfeeding
Acute heart failure

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Partial pressure of carbon dioxide. Timepoint: Before the intervention, 24 hours after the intervention and 48 hours after the intervention. Method of measurement: Through blood sampling and blood gas analysis.

Secondary Outcome Measures

Name	Time	Method
Oxygen saturation. Timepoint: Before the intervention, 24 hours after the intervention and 48 hours after the intervention. Method of measurement: Through blood sampling and blood gas analysis.