Intermittent CPAP in hypoxemic COVID patients

Not Applicable

Recruiting

• Conditions: COVID-19 Infection.; Pneumonia due to SARS-associated coronavirus; J12.81

• Registration Number: IRCT20200723048178N2
• Lead Sponsor: Pakistan Institute of Medical Sciences, Islamabad

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

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

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 93

Inclusion Criteria

Hospitalized patients with severe COVID-19 infection
Patients requiring supplemental oxygen of 10 litres or more

Exclusion Criteria

Unco-operative patient
Patients with Pneumothorax
Patients with Surgical emphysema
GCS less than 13
Excessive respiratory secretions
Shock

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
In-hospital mortality. Timepoint: 28 days after intervention. Method of measurement: A Questionnaire will be used to record the data.

Secondary Outcome Measures

Name	Time	Method
The duration of hospital stay. Timepoint: 28 days following the intervention. Method of measurement: A Questionnaire will be used to record the data.;The use of non-invasive or invasive mechanical ventilation. Timepoint: 28 days after intervention. Method of measurement: A Questionnaire will be used to record the data.