Skip to main content
TTrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor.
RECRUITINGOBSERVATIONAL

Study of Progression of Community Acquired Pneumonia in the Hospital in Patients With More Severe Preexisting Diseases and Immunosuppression

Study of Progression of Hospitalized Community Acquired Pneumonia - Genetic Resistance and Susceptibility for the Evolution of Severe Sepsis in Patients With More Severe Preexisting Diseases and Immunosuppression to Complement the PROGRESS CAP Cohort

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Pneumonia is a common infectious disease of the lung, often requiring treatment in the hospital. Clinical scoring systems are available, identifying patients not requiring hospitalization. However, the course of disease of patients in the hospital remains hard to predict. While most patients will recover quickly, some will, despite appropriate treatment, develop a severe course leading to sepsis and systemic responses resulting in organ dysfunction. The PROGRESS consortium aims to identify clinical, genetic, and other molecular markers and combinations there of predicting a severe course of pneumonia in the hospital. Such predictors will, for instance, support decisions on earlier transfer of patients to intensive care and thus improving outcome. PROGRESS-COMORB aims to extend findings from the previous PROGRESS study to patients with more severe preexisting conditions and immunosuppression.

Who May Be Eligible (Plain English)

Who May Qualify: 1. Hospitalization with community acquired pneumonia (CAP) confirmed by pulmonary infiltrate in chest imaging 2. Valid willing to sign a consent form form 3. Working diagnosis of CAP by enrolling physician 4. No hospitalization for any reason within 28 days prior to hospitalization for the current episode of CAP 5. At least 2 out of the five following clinical symptoms: - Fever - Cough - Purulent sputum - Shortness of breath or need for respiratory support - Crackling or rales on auscultation, dullness to percussion, or bronchial breathing 6. At least 1 of the following criteria - Known HIV infection or AIDS - Anti-tumor treatment within the past six months - Therapy with corticosteroids ≥ 20mg for ≥ 14 days before enrollment - Non-steroidal immunosuppressive therapy within the past six months - Cytostatic therapy within the past six months - Radiation therapy within the past six months - Bone marrow transplant received - Respiratory support at home via tracheostoma - Cystic fibrosis - Heart failure: New York Heart Association (NYHA) Stadium IV or HFrEF (defined as left ventricular ejection fraction \<40%). - Decompensated liver disease (Child-Pugh class C) - Diabetes mellitus with HbA1c ≥ 8,5 % - End-stage renal disease requiring dialysis - Pulmonary hypertension (all classes) with mPAP \> 20 mmHg (right heart catheter) Who Should NOT Join This Trial: 1. Participation in this study at an earlier time 2. More than 48 hours in the hospital before enrollment (for patients directly to intensive care: more than 7 days) 3. Pregnancy 4. Breastfeeding 5. Active tuberculosis 6. Acute lung injury or acute respiratory distress syndrome for extrapulmonary reasons 7. Massive aspiration 8. Sepsis with extrapulmonary focus 9. Acute pulmonary embolism Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: 1. Hospitalization with community acquired pneumonia (CAP) confirmed by pulmonary infiltrate in chest imaging 2. Valid informed consent form 3. Working diagnosis of CAP by enrolling physician 4. No hospitalization for any reason within 28 days prior to hospitalization for the current episode of CAP 5. At least 2 out of the five following clinical symptoms: * Fever * Cough * Purulent sputum * Shortness of breath or need for respiratory support * Crackling or rales on auscultation, dullness to percussion, or bronchial breathing 6. At least 1 of the following criteria * Known HIV infection or AIDS * Anti-tumor treatment within the past six months * Therapy with corticosteroids ≥ 20mg for ≥ 14 days before enrollment * Non-steroidal immunosuppressive therapy within the past six months * Cytostatic therapy within the past six months * Radiation therapy within the past six months * Bone marrow transplant received * Respiratory support at home via tracheostoma * Cystic fibrosis * Heart failure: New York Heart Association (NYHA) Stadium IV or HFrEF (defined as left ventricular ejection fraction \<40%). * Decompensated liver disease (Child-Pugh class C) * Diabetes mellitus with HbA1c ≥ 8,5 % * End-stage renal disease requiring dialysis * Pulmonary hypertension (all classes) with mPAP \> 20 mmHg (right heart catheter) Exclusion Criteria: 1. Participation in this study at an earlier time 2. More than 48 hours in the hospital before enrollment (for patients directly to intensive care: more than 7 days) 3. Pregnancy 4. Breastfeeding 5. Active tuberculosis 6. Acute lung injury or acute respiratory distress syndrome for extrapulmonary reasons 7. Massive aspiration 8. Sepsis with extrapulmonary focus 9. Acute pulmonary embolism

Locations (10)

Charité - Universitätsmedizin Berlin, Medizinische Klinik m. S. Infektiologie und Pneumologie
Berlin, Germany
Humboldt-Klinikum Vivantes, Kardiologie und kons. Intensivmedizin
Berlin, Germany
Gemeinschaftskrankenhaus Havelhöhe, Kardio-Pneumologie
Berlin, Germany
Städtisches Klinikum Dessau, Innere Medizin
Dessau, Germany
Universitätsklinikum Hamburg Eppendorf, Onkologisches Zentrum, Pneumologische Studienzentrale
Hamburg, Germany
Universitätsklinikum Leipzig, Klinik für Onkologie, Gastroenterologie, Hepatologie, Pneumologie
Leipzig, Germany
Klinikum St. Georg gGmbH, Klinik für Infektions-/Tropenmedizin und Nephrologie
Leipzig, Germany
Universitätsklinikum Gießen und Marburg, Klinik für Pneumologie und Anästhesie
Marburg, Germany
Universitätsklinikum Münster, Kardiologie 1
Münster, Germany
Diakoniekrankenhaus Rotenburg(Wümme)gGmbH, Zentrum für Pneumologie
Rotenburg (Wümme), Germany