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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02139163
Other study ID # U1111-1147-8393
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 2002
Est. completion date January 2022

Study information

Verified date July 2020
Source Hannover Medical School
Contact Tobias Welte, Prof.
Phone +49-511-532-5927
Email office@capnetz.de
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Long-term objectives of the basic research part are improvement of CAP-management with respect to therapy, diagnosis and prevention to contribute to a better care of patients with pneumonia.


Description:

Long-term objectives of the basic research part are improvement of CAP-management with respect to therapy, diagnosis and prevention to contribute to a better care of patients with pneumonia. The aim of the study CAPNETZ is to improve diagnosis, treatment and patient care.


Recruitment information / eligibility

Status Recruiting
Enrollment 10150
Est. completion date January 2022
Est. primary completion date January 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cohort Study


Locations

Country Name City State
Germany CAPNETZ FOUNDATION Hannover Medical School (MHH) Hannover Niedersachsen
Germany Hannover Medical School Hannover Niedersachsen

Sponsors (1)

Lead Sponsor Collaborator
Hannover Medical School

Country where clinical trial is conducted

Germany, 

References & Publications (6)

Ewig S, Klapdor B, Pletz MW, Rohde G, Schütte H, Schaberg T, Bauer TT, Welte T; CAPNETZ study group. Nursing-home-acquired pneumonia in Germany: an 8-year prospective multicentre study. Thorax. 2012 Feb;67(2):132-8. doi: 10.1136/thoraxjnl-2011-200630. Epu — View Citation

Klapdor B, Ewig S, Pletz MW, Rohde G, Schütte H, Schaberg T, Welte T; CAPNETZ Study Group. Community-acquired pneumonia in younger patients is an entity on its own. Eur Respir J. 2012 May;39(5):1156-61. doi: 10.1183/09031936.00110911. Epub 2011 Nov 16. Er — View Citation

Klapdor B, Ewig S, Schaberg T, Rohde G, Pletz MW, Schütte H, Welte T; CAPNETZ study group. Presentation, etiology and outcome of pneumonia in younger nursing home residents. J Infect. 2012 Jul;65(1):32-8. doi: 10.1016/j.jinf.2012.02.003. Epub 2012 Feb 10. — View Citation

Kolditz M, Höffken G, Martus P, Rohde G, Schütte H, Bals R, Suttorp N, Pletz MW; CAPNETZ study group. Serum cortisol predicts death and critical disease independently of CRB-65 score in community-acquired pneumonia: a prospective observational cohort stud — View Citation

Lepper PM, Ott S, Nüesch E, von Eynatten M, Schumann C, Pletz MW, Mealing NM, Welte T, Bauer TT, Suttorp N, Jüni P, Bals R, Rohde G; German Community Acquired Pneumonia Competence Network. Serum glucose levels for predicting death in patients admitted to — View Citation

Zobel K, Martus P, Pletz MW, Ewig S, Prediger M, Welte T, Bühling F; CAPNETZ study group. Interleukin 6, lipopolysaccharide-binding protein and interleukin 10 in the prediction of risk and etiologic patterns in patients with community-acquired pneumonia: — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary diagnosis Assessment of diagnosis:
Patients will be asked for example, about their diagnosis, comorbidities, specific risk factors and pneumonia symptoms.
2 weeks
Primary therapy Assessment of therapy:
Patients will be asked about their therapy due to pneumonia symptoms, previous therapy, medication History etc.
2 weeks
Primary hospitalization Assessment of hospitalization:
Patients will be asked about hospitalization, date, time and duration of hospitalization due to pneumonia symptoms.
2 weeks
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