Actively Recruiting
Long-term Changes in Host-Microbiome Interactions and Progression of Cardiovascular and Respiratory Diseases After Pneumonia The HOMI-LUNG Project on Hospital-Acquired Pneumonia
Led by Nantes University Hospital · Updated on 2025-01-17
300
Participants Needed
5
Research Sites
225 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the long-term effects of pneumonia on cardiovascular and respiratory diseases within the HOMI-LUNG project, funded by Horizon Europe. This international project focuses on understanding how respiratory infections like pneumonia may lead to worsening heart and lung conditions. It aims to measure the impact of cardiovascular disease after pneumonia, explore patients' acceptance of lasting health changes, and identify pneumonia subtypes linked to worsening cardiovascular disease. The study involves collecting blood samples and oropharyngeal swabs at several times: at the start, 6 months, 18 months, and 30 months, with some groups having fewer samples. Participants undergo various tests including ECGs at the same intervals, and assessments of respiratory and heart function through exercise tests, spirometry, plethysmography, and carbon monoxide absorption tests at the start, 6 months, and 30 months. A CT scan to measure calcium in arteries is performed at 30 months to evaluate individual cardiovascular risk. Participants will be monitored over 30 months with repeated clinical evaluations and laboratory tests to track changes in heart and lung health. Outcomes measured include major adverse cardiovascular events within 6 months and poor cardiorespiratory fitness after 30 months. The study involves detailed assessments to understand disease progression and long-term health alterations after pneumonia, ensuring safety and comprehensive follow-up throughout the participation period.
CONDITIONS
Official Title
Long-term Alterations of Host-microbiome Interactions and Cardiovascular and Respiratory Diseases Progression After Pneumonia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female aged 40 years or older
- Hospitalized for acute coronary syndrome less than 7 days ago (Group A)
- Undergoing coronary artery bypass surgery and hospitalized in intensive care unit for more than 12 hours (Group B)
- Familial high cholesterol or triglycerides with no personal cardiovascular disease and recent negative cardiac exercise test within 12 months (Group C)
- At least one cardiovascular disease risk factor and recovered from mechanically ventilated hospital-acquired pneumonia during current hospitalization (Group D)
- Provided informed consent
- Covered by a health insurance plan
You will not qualify if you...
- Older than 80 years
- Immunosuppression before current hospital stay (including low lymphocyte count, blood cancers, aplasia, recent chemotherapy/radiotherapy, or anti-graft rejection drugs)
- Pregnant or breastfeeding women
- Adults under guardianship or trusteeship
- Low chance of survival at 28 days
- History of community-acquired or hospital-acquired pneumonia within the last year (Groups A, B, C)
AI-Screening
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Trial Site Locations
Total: 5 locations
1
Angers University Hospital
Angers, France
Not Yet Recruiting
2
Nantes University Hospital
Nantes, France
Actively Recruiting
3
Rennes University Hospital
Rennes, France
Not Yet Recruiting
4
Rouen University Hospital
Rouen, France
Not Yet Recruiting
5
Toulouse University Hospital
Toulouse, France
Not Yet Recruiting
Research Team
A
Antoine ROQUILLY
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
4
Frequently Asked Questions
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