Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients (aged between 18 and 75y) with laboratory confirmed diagnosis of COVID-19 pneumonia, presenting with self-reported symptom of shortness of breath will be included in this trial after informed written consent
Exclusion criteria
Exclusion criteria: Patients who refuse to participate, hemodynamically unstable patients, pregnant patients and patients requiring mechanical ventilation will be excluded from this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare repeated positioning with 4h continuous prone positioning in terms of self-reported dyspnea in a 10- point visual analogue scaleTimepoint: 4hour since randomization | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To compare both the techniques in terms of oxygenation status (room air oxyhemoglobin saturation or PaO2/FiO2 ratio in arterial blood gas) 2. To compare the requirement of rescue therapy (high flow nasal oxygen) in both the groups. 3. To compare hemodynamic variables in both the groups. 4. To compare the requirement of mechanical ventilation within 24h in both the groups. 5. To compare the change in respiratory rate in both the groups. Timepoint: 4 hour since randomization | — |
Countries
India
Contacts
All India Institute of Medical Sciences, New Delhi