Covid-19. Coronavirus infection, unspecified
Conditions
Interventions
Intervention 1: Intervention group: In this research, the CPAP device of Saadat and venet manufacturers is used. Using an air pump, the CPAP device transmits airflow to the patient at a pressure set b
Adjustable pressure range: 20 - 4 cm water
Pressure adjustment: 3 - 0 cm of water
Adjustable initial pressure by the patient
Device settings with buttons
LED lights on the device
Storing, calculating and retrieving information is like the average total treatment hours. Intervention 2: Intervention group: In this research, the BIPAP device of Fisher and Resmed manufacturers is
Sponsors
Gonabad University of Medical Sciences
Vice Chancellor for Research, Gonabad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Willingness to participate in the study Age 20 -60 y/o No history of cardiovascular disease such as hypertension, liver, kidney according to self-declaration Need to prescribe oxygen and candidate for non-invasive respiratory assistance (NIV) according to physician (no need for intubation) No ban on the use of masks Definitive diagnosis of coronavirus infection by physician and laboratory results
Exclusion criteria
Exclusion criteria: Need to intubate the patient immediately Awareness level based on the Glasgow scale less than 15 Any change in the patient's condition that affects the course of treatment, for example blood pressure below 90 mmhg despite fluid therapy or the use of vasopressors
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean score of hemodynamic parameters. Timepoint: Before the mask is prescribed, it will be examined by a person immediately after use and after 1 hour, 6 hours and then daily for up to 3 days at a specific time. Method of measurement: Patient-connected monitoring device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Mean oxygen saturation, mean blood pressure, mean pulse rate. Timepoint: Based on the monitor attached to the patient before the mask is administered, immediately after use and after 1 hour, 6 hours and then daily for up to 3 days at a specific time will be examined by one person. Method of measurement: Patient-connected monitoring device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Kokab Basiri Moghaddam
Gonabad University of Medical Sciences
Outcome results
None listed