Epidemiological Study on Community Acquired Pneumonia (CAPNETZ)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT02139163 |
Recruitment Status :
Recruiting
First Posted : May 15, 2014
Last Update Posted : July 31, 2020
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Condition or disease | Intervention/treatment |
---|---|
Community Acquired Pneumonia | Other: Cohort Study |
Study Type : | Observational [Patient Registry] |
Estimated Enrollment : | 10150 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Target Follow-Up Duration: | 6 Months |
Official Title: | Epidemiological Study on Community Acquired Pneumonia |
Study Start Date : | October 2002 |
Estimated Primary Completion Date : | January 2021 |
Estimated Study Completion Date : | January 2022 |
Group/Cohort | Intervention/treatment |
---|---|
patients with pneumonia |
Other: Cohort Study |
- diagnosis [ Time Frame: 2 weeks ]
Assessment of diagnosis:
Patients will be asked for example, about their diagnosis, comorbidities, specific risk factors and pneumonia symptoms.
- therapy [ Time Frame: 2 weeks ]
Assessment of therapy:
Patients will be asked about their therapy due to pneumonia symptoms, previous therapy, medication History etc.
- hospitalization [ Time Frame: 2 weeks ]
Assessment of hospitalization:
Patients will be asked about hospitalization, date, time and duration of hospitalization due to pneumonia symptoms.

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- age ≥ 18
- infiltrate on chest X-ray
- further Inclusion criteria: cough or production of purulent sputum or pathologic lung auscultation (crackles) or fever
Exclusion Criteria:
- hospital inpatient treatment within the last 28 days
- Immune suppressed patients

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02139163
Contact: Tobias Welte, Prof. | +49-511-532-5927 | office@capnetz.de |
Germany | |
CAPNETZ FOUNDATION Hannover Medical School (MHH) | Recruiting |
Hannover, Niedersachsen, Germany, 30625 | |
Contact: Abrahamczik +49-(0)511-532-5927 Abrahamczik.margarete@mh-hannover.de | |
Contact: Kroener +49-(0)511-532-4447 Kroener.Waldemar@mh-hannover.de | |
Principal Investigator: Tobias Welte, Prof. | |
Hannover Medical School | Recruiting |
Hannover, Niedersachsen, Germany, 30625 | |
Contact: Tobias Welte, Prof. +49-511-532-5927 office@capnetz.de |
Study Chair: | Tobias Welte, Prof. Dr. | Hannover Medical School |
Publications of Results:
Responsible Party: | Hannover Medical School |
ClinicalTrials.gov Identifier: | NCT02139163 |
Other Study ID Numbers: |
U1111-1147-8393 |
First Posted: | May 15, 2014 Key Record Dates |
Last Update Posted: | July 31, 2020 |
Last Verified: | July 2020 |
Community acquired pneumonia CAP CAPNETZ age ≥18 |
infiltrate on chest X-ray cough or production of purulent sputum pathologic lung auscultation fever |
Pneumonia Lung Diseases Respiratory Tract Diseases Respiratory Tract Infections |