Epidemiological Study on Community Acquired Pneumonia (CAPNETZ)
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ClinicalTrials.gov Identifier: NCT02139163 |
Recruitment Status :
Recruiting
First Posted : May 15, 2014
Last Update Posted : July 31, 2020
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Sponsor:
Hannover Medical School
Information provided by (Responsible Party):
Hannover Medical School
Tracking Information | |||||
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First Submitted Date | January 24, 2014 | ||||
First Posted Date | May 15, 2014 | ||||
Last Update Posted Date | July 31, 2020 | ||||
Study Start Date | October 2002 | ||||
Estimated Primary Completion Date | January 2021 (Final data collection date for primary outcome measure) | ||||
Current Primary Outcome Measures |
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Original Primary Outcome Measures | Same as current | ||||
Change History | |||||
Current Secondary Outcome Measures | Not Provided | ||||
Original Secondary Outcome Measures | Not Provided | ||||
Current Other Pre-specified Outcome Measures | Not Provided | ||||
Original Other Pre-specified Outcome Measures | Not Provided | ||||
Descriptive Information | |||||
Brief Title | Epidemiological Study on Community Acquired Pneumonia | ||||
Official Title | Epidemiological Study on Community Acquired Pneumonia | ||||
Brief 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. | ||||
Detailed 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. | ||||
Study Type | Observational [Patient Registry] | ||||
Study Design | Observational Model: Cohort Time Perspective: Prospective |
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Target Follow-Up Duration | 6 Months | ||||
Biospecimen | Not Provided | ||||
Sampling Method | Non-Probability Sample | ||||
Study Population | patients with pneumonia | ||||
Condition | Community Acquired Pneumonia | ||||
Intervention | Other: Cohort Study | ||||
Study Groups/Cohorts | patients with pneumonia
Intervention: Other: Cohort Study
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Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | |||||
Recruitment Status | Recruiting | ||||
Estimated Enrollment |
10150 | ||||
Original Estimated Enrollment | Same as current | ||||
Estimated Study Completion Date | January 2022 | ||||
Estimated Primary Completion Date | January 2021 (Final data collection date for primary outcome measure) | ||||
Eligibility Criteria | Inclusion Criteria:
Exclusion Criteria:
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Sex/Gender |
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Ages | 18 Years and older (Adult, Older Adult) | ||||
Accepts Healthy Volunteers | No | ||||
Contacts |
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Listed Location Countries | Germany | ||||
Removed Location Countries | |||||
Administrative Information | |||||
NCT Number | NCT02139163 | ||||
Other Study ID Numbers | U1111-1147-8393 | ||||
Has Data Monitoring Committee | No | ||||
U.S. FDA-regulated Product | Not Provided | ||||
IPD Sharing Statement | Not Provided | ||||
Responsible Party | Hannover Medical School | ||||
Study Sponsor | Hannover Medical School | ||||
Collaborators | Not Provided | ||||
Investigators |
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PRS Account | Hannover Medical School | ||||
Verification Date | July 2020 |