Clinical Trials Directory

Trials / Unknown

UnknownNCT04860687

Quality of Life After COVID-19 Related Acute respIratory Distress Syndrome Among ICU Survivors Patients in Italy: the ODISSEA Study.

Status
Unknown
Phase
Study type
Observational
Enrollment
309 (estimated)
Sponsor
Azienda Sanitaria-Universitaria Integrata di Udine · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Acute respiratory insufficiency is one of the principal causes of intensive care admission for COVID 19 positive patients. This may determine a variable mortality rate ranging from 25-30%. In these patients, many days of non-invasive or invasive mechanical ventilation are needed to correct severe hypoxemia. Mechanical ventilation is not a direct therapy but allows the clinicians to prolong the "time-to-recovery" interval necessary for COVID 19 respiratory insufficiency treatment. Long intensive care stay, mechanical ventilation, the use of steroids and sedatives have an impact on the survivors. Previous studies demonstrated that patients admitted to intensive care with non-COVID acute respiratory distress syndrome had a reduction in the quality of life even up to one year after discharge. The aim of this study is to understand if COVID-19 related acute respiratory distress syndrome has a worse impact on the quality of life one year after discharge when compared with non-COVID-19 acute respiratory distress syndrome.

Conditions

Timeline

Start date
2021-08-01
Primary completion
2021-11-30
Completion
2021-12-31
First posted
2021-04-27
Last updated
2021-10-07

Locations

8 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT04860687. Inclusion in this directory is not an endorsement.