Status:

RECRUITING

Long-term Alterations of Host-microbiome Interactions and Cardiovascular and Respiratory Diseases Progression After Pneumonia

Lead Sponsor:

Nantes University Hospital

Conditions:

Hospital Acquired Pneumonia (HAP)

Cardiovascular and Respiratory Disease

Eligibility:

All Genders

40-80 years

Phase:

NA

Brief Summary

The HOMI-LUNG - HAP study is part of the HOMI-LUNG project, funded by the Horizon Europe program. The "HOMI-LUNG" project is an international, interdisciplinary project that aims to better understand ...

Eligibility Criteria

Inclusion

  • Group A (patients with acute cardiac disease)
  • Male or female
  • Age ≥ 40years old
  • Hospitalized for acute coronary syndrome for less than 7 days.
  • Informed consent from the patient
  • Person insured under a health insurance scheme
  • Group B (patients with chronic cardiovascular disease)
  • Male or female,
  • Age ≥ 40 years old
  • Undergoing coronary artery by-pass surgery
  • Hospitalized in intensive care unit for \> 12 hours
  • Informed consent from the patient
  • Person insured under a health insurance scheme
  • Group C (patients at risk of CVRD without chronic cardiovascular disease)
  • Male or female,
  • Age ≥ 40 years old
  • Familial high levels of cholesterol or triglycerides
  • With no personal history of CVRD, with a recent negative cardiac exercise test (last test inferior to 12 months)
  • Follow-up for lipid abnormalities at high risk of CVRD events
  • Informed consent from the patient
  • Person insured under a health insurance scheme
  • Group D (patients with HAP)
  • Male or female
  • Age ≥ 40years old
  • With one or more risk factors for CVD among:
  • smoking, abnormal lipidic levels, high blood pressure, obesity, diabetes mellitus, chronic kidney disease
  • Cured from mechanically ventilated HAP during the current hospitalization
  • Informed consent from the patient or relatives
  • Person insured under a health insurance scheme

Exclusion

  • o Groups A, B, C and D
  • Age \>80 years old
  • Immunosuppression pre-existing to the index hospitalisation, defined as lymphopenia \< 500 elements/mm3, haematologic cancer, aplasia, chemotherapy/radiotherapy for cancer within 3 months prior to the inclusion, or anti-graft rejection drug.
  • Pregnant women, breastfeeding women.
  • Adults under guardianship or trusteeship.
  • Low probability of survival at day 28.
  • o Groups A, B, C
  • Community-acquired pneumonia or Hospital-acquired pneumonia within the last year.

Key Trial Info

Start Date :

January 2 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 1 2029

Estimated Enrollment :

300 Patients enrolled

Trial Details

Trial ID

NCT06602934

Start Date

January 2 2025

End Date

May 1 2029

Last Update

January 17 2025

Active Locations (5)

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Page 1 of 2 (5 locations)

1

Angers University Hospital

Angers, France

2

Nantes University Hospital

Nantes, France

3

Rennes University Hospital

Rennes, France

4

Rouen University Hospital

Rouen, France