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UnknownNCT04098094

Outcomes of RV Dysfunction in Acute Exacerbation of Chronic Respiratory Diseases

Prevalence of Right Ventricular Dysfunction in Acute Exacerbation of Chronic Respiratory Diseases and Its Impact on Outcomes

Status
Unknown
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Observational study in patients with chronic respiratory diseases (chronic obstructive pulmonary diseases, bronchiectasis, interstitial lung diseases, neuromuscular diseases, obesity-hypoventilation syndrome...) admitted in intensive care unit for acute respiratory failure. The main objective is to determine the prevalence of right ventricular (RV) dysfunction in this population and to analyze the impact of such a complication on outcomes (survival at day-28, duration of non-invasive or mechanical ventilation, duration of hospital stay). RV function will be assessed by echocardiography at admission, after 3 days and at discharge. Plasma NT-proBNP and troponin levels will be collected.

Detailed description

Observational study in patients with chronic respiratory diseases (chronic obstructive pulmonary diseases, bronchiectasis, interstitial lung diseases, neuromuscular diseases, obesity-hypoventilation syndrome...) admitted in intensive care unit for acute respiratory failure. Inclusion Criteria: * Chronic respiratory disease (COPD, ILD, OHS...) * Admission in ICU for acute respiratory failure * Patient's non-opposition Exclusion Criteria: * Patients \< 18 year-old * Protected patients * Pregnant women The main objective is to determine the prevalence of right ventricular (RV) dysfunction in this population and to analyze the impact of such a complication on outcomes (survival at day-28, duration of non-invasive or mechanical ventilation, duration of hospital stay). RV function will be assessed by echocardiography at admission, after 3 days and at discharge. Plasma NT-proBNP and troponin levels will be collected.

Conditions

Timeline

Start date
2019-09-19
Primary completion
2022-10-30
Completion
2022-10-30
First posted
2019-09-23
Last updated
2022-02-18

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04098094. Inclusion in this directory is not an endorsement.