Actively Recruiting
Longitudinal Recovery Trajectories After an Acute Respiratory Distress Syndrome, a New Understanding
Led by Institut de Recerca Biomèdica de Lleida · Updated on 2024-03-06
246
Participants Needed
3
Research Sites
183 weeks
Total Duration
On this page
Sponsors
I
Institut de Recerca Biomèdica de Lleida
Lead Sponsor
I
Instituto de Salud Carlos III
Collaborating Sponsor
AI-Summary
What this Trial Is About
COVID-19 resulted in the largest cohort of critical illness survivors in history, heightened awareness of the importance of the respiratory sequelae after an acute distress respiratory syndrome (ADRS). Despite the advancement of acute-phase ARDS management, it is unknown whether there are differences in the longitudinal recovery trajectories between patients with post-ARDS due to COVID-19 and due to other causes. The main objective of the study is to identify risk factors of pulmonary sequela (lung diffusing capacity) at long-term follow-up in survivors of ARDS. The investigators are also interested in describing the long-term longitudinal recovery trajectories at a multi-dimensional level (symptoms, quality of life, neurocognitive, other lung function parameters, exercise capacity, chest imaging and molecular profiles) of ARDS survivors, and compared between ARDS caused by COVID-19. The ultimate goal is to understand the pathobiological mechanisms associated with a severe lung injury at the long term, allowing the introduction of clinical guidelines for the management of post-ARDS patients and the assignment of personalized interventions.
CONDITIONS
Official Title
Longitudinal Recovery Trajectories After an Acute Respiratory Distress Syndrome, a New Understanding
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male and female patients aged 6518 years
- Admission to the ICU
- Diagnosis of severe pneumonia and/or acute respiratory distress syndrome (ARDS) based on the 2023 definition due to any cause (infectious or non-infectious)
You will not qualify if you...
- Life expectancy less than one year
- Transfer to another hospital during hospitalization or follow-up
- Stay in palliative care
- Severe mental disability preventing pulmonary function tests during follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Hospital de Tortosa Verge de la Cinta
Tortosa, Tarragona, Spain, 43500
Actively Recruiting
2
Hospital Universitari Arnau de Vilanova
Lleida, Spain, 25198
Actively Recruiting
3
Hospital Universitari Joan XXIII
Tarragona, Spain, 43005
Actively Recruiting
Research Team
J
Jessica González Gutiérrez, MD, PhD
CONTACT
F
Ferran Barbé Illa, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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