Medical School Hannover
Hanover, 30625, Germany
Location status: Recruiting
NCT Number: NCT02139163
The main objective of this study is to investigate prevalence and risk factors for community-acquired pneumonia (CAP) and its interaction with comorbidities in an unselected group of adult patients receiving outpatient and inpatient care. In addition, information on HIV as a risk factor for CAP and on CAP in immunocompromised patients is collected.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Hanover, 30625, Germany
Location status: Recruiting
The CAPNETZ study is a prospective, multicenter observational study investigating community-acquired pneumonia (CAP). Patients are recruited from outpatient and inpatient settings at hospitals and from primary care physicians (primarily specialists) and are followed for a period of six months. All CAP patients who meet the inclusion and exclusion criteria, consent to participate, and in whom the presence of a newly developed, community-acquired pneumonia can be verified are invited to participate. The baseline examination includes a detailed medical history, medication history, and a physical examination to record clinical and vital signs. In addition, the results of routine clinical imaging are documented, and biosamples (blood, urine, and respiratory specimens) are collected for clinical chemistry and microbiological analysis. Further in-person visits to document the course of the disease and treatment, including the collection of additional blood samples, take place 3 and 7 days after study enrollment. Twenty-eight days after enrollment, the patient's health status, treatment course, and complications are assessed by telephone. Finally, after 180 days, a telephone survey is conducted to determine the patient's whereabouts and survival status. Apart from the collection of biomaterials, no interventions are required or planned; physicians treat their patients as they normally would.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 2 weeks
Assessment of diagnosis:
Patients will be asked for example, about their diagnosis, comorbidities, specific risk factors and pneumonia symptoms.
Time frame: 2 weeks
Assessment of therapy:
Patients will be asked about their therapy due to pneumonia symptoms, previous therapy, medication History etc.
Time frame: 2 weeks
Assessment of hospitalization:
Patients will be asked about hospitalization, date, time and duration of hospitalization due to pneumonia symptoms.
Contact information is provided by the study sponsor or research team.
Frank Eberhardt
CONTACT
Waldemar Kröner
CONTACT
Capnetz Stiftung
Other
Acronym: CAPNETZ
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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