Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06601998

Cardiovascular Disease Progression in Survivors of Community Acquired Pneumonia and COVID-19 Lung Infection A Non-interventional, Prospective, Cross-sectional Study

Led by Hellenic Institute for the Study of Sepsis · Updated on 2026-02-17

650

Participants Needed

17

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the progression of cardiovascular diseases in people who have survived community-acquired pneumonia, including infections from influenza and COVID-19. The study aims to understand how pneumonia and infections affect the risk of serious cardiovascular events like stroke and heart attack. It focuses on how the body's immune response and changes in the microbiome (the community of microorganisms in the body) influence disease progression, with the goal of identifying patients at higher risk and developing personalized treatments. The study observes different groups including healthy controls, individuals with cardiovascular risk factors but no severe pneumonia history, survivors of severe COVID-19 pneumonia, and survivors of severe community-acquired pneumonia. Participants undergo various assessments such as blood sampling for immune and genetic analysis, lung function tests, heart ultrasounds, ECGs, six-minute walk tests, and completion of symptom questionnaires. These evaluations occur over an extended period to monitor recovery and disease progression. Participants will be followed for up to 36 months after enrollment. Researchers will track major cardiovascular events and cardiorespiratory fitness at 6 and 36 months, along with hospitalizations, respiratory complications, quality of life, mental health, metabolic diseases, and lung and heart function. The study includes detailed monitoring of immune responses, microbiome changes, and physical health measures to better understand long-term effects after pneumonia and to identify biomarkers predicting treatment response and cardiovascular disease progression.

CONDITIONS

Brief Title

Cardiovascular Disease Progression in Survivors of Community Acquired Pneumonia and Lung Infection by Covid-19.

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older of both genders
  • No history of severe pneumonia for healthy controls
  • Healthy controls may have no or one of these: obesity (BMI >35), type 2 diabetes, high cholesterol, high blood pressure, or family history of cardiovascular disease
  • Cardiovascular risk controls must have at least two of the listed comorbidities and no severe pneumonia history
  • Survivors of severe COVID-19 pneumonia treated with dexamethasone
  • Survivors of severe community-acquired pneumonia treated with antibiotics
Not Eligible

You will not qualify if you...

  • Presence of two or more comorbidities for healthy controls
  • Any co-existing disorders causing cardiovascular symptoms
  • Limited chance of survival for at least six months due to other medical conditions
  • Pregnancy or breastfeeding
  • History of severe congestive heart failure (Stage III-IV) for pneumonia survivors
  • History of severe dyspnea (Stage III or IV) before pneumonia for pneumonia survivors
  • Same survival limitation and pregnancy criteria apply to all groups
  • Exclusion criteria vary slightly by group as detailed above

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - At enrollment and hospital discharge (approximately 1 month after enrollment)

Participants undergo assessments including blood samples, oropharyngeal swabs, six-minute walk test, spirometry, ECG, heart ultrasound, cardiopulmonary exercise stress testing, and symptom questionnaires to evaluate cardiovascular and respiratory health after pneumonia or COVID-19 infection.

1 to 2 visits depending on the assessments

Long-term Monitoring

Duration - Up to 36 months

Participants are followed to monitor cardiovascular disease events, cardiorespiratory fitness, hospitalizations, respiratory complications, metabolic disease, and quality of life changes over time after pneumonia or COVID-19 recovery.

Visits at Month 6, Month 18, and Month 36 for follow-up assessments

Trial Site Locations

Total: 17 locations

1

2nd Department of Internal Medicine, University General Hospital of Alexandroupolis

Alexandroupoli, Greece

Not Yet Recruiting

2

10th Department of Pulmonary Medicine, Sotiria Athens Hospital of Chest Diseases

Athens, Greece

Actively Recruiting

3

1st Department of Internal Medicine, General Hospital of Athens G. GENNIMATAS

Athens, Greece

Actively Recruiting

4

1st Department of Internal Medicine, General Hospital of Athens KORGIALENIO-BENAKIO E.E.S.

Athens, Greece

Actively Recruiting

5

1st Department of Internal Medicine, General Hospital of Voula ASKLEPIEIO

Athens, Greece

Actively Recruiting

6

1st Intensive Care Clinic of the Medical School of the University of Athens, Evangelismos General Hospital

Athens, Greece

Actively Recruiting

7

1st University Department of Internal Medicine, General Hospital of Athens LAIKO

Athens, Greece

Actively Recruiting

8

1st University Department of Pulmonary Medicine, Sotiria Athens Hospital of Chest Diseases

Athens, Greece

Actively Recruiting

9

2nd Department of Pulmonary Medicine, Sotiria Athens Hospital of Chest Diseases

Athens, Greece

Actively Recruiting

10

3rd University Department of Internal Medicine, Sotiria Athens Hospital of Chest Diseases

Athens, Greece

Actively Recruiting

11

4th Department of Internal Medicine, ATTIKON University General Hospital

Athens, Greece

Actively Recruiting

12

Intensive Care Unit, General Hospital of Voula ASKLEPIEIO

Athens, Greece

Actively Recruiting

13

Out-patients clinic, General Hospital of Voula ASKLEPIEIO

Athens, Greece

Actively Recruiting

14

1st Department of Internal Medicine, Thriasio General Hospital of Elefsina

Elefsina, Greece

Not Yet Recruiting

15

1st Department of Internal Medicine, AHEPA University General Hospital of Thessaloniki

Thessaloniki, Greece

Not Yet Recruiting

16

Intensive Care Unit 2, AHEPA University General Hospital of Thessaloniki

Thessaloniki, Greece

Not Yet Recruiting

17

Intensive Care Unit, "Ippokrateion" General Hospital of Thessaloniki

Thessaloniki, Greece

Not Yet Recruiting

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Research Team

P

Prof. Evangelos Giamarellos-Bourboulis

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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