Recruiting NCT04666246
Inspiratory Effort in COVID-19
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Acute Respiratory Failure, Covid19. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Inspiratory Effort Assessment in Patients With COVID-19 Pneumonia Undergoing Non Invasive Respiratory Support
Overview
This study aims at assessing esophageal pressure in patients with acute respiratory failure due to COVID-19 undergoing non invasive respiratory support.
Primary outcome measures
- Inspiratory effort quantification [Time frame: 24 hours from admission]
Secondary outcome measures (1)
- Non invasive respiratory support failure [Time frame: 24 hours]
Eligibility criteria
Inclusion criteria
- COVID-19
- Acute respiratory failure undergoing non-invasive respiratory support
Exclusion criteria
- Need for immediate endotracheal intubation
- Chronic respiratory diseases
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Italy · 1 center
- University Hospital of Modena — Modena
Identifiers
NCT: NCT04666246 · UModenaReggio17