Official Title
Intersectoral Platform (SÜP) of the National Pandemic Cohort Network (NAPKON)
Brief Summary

The intersectoral platform is part of the National Pandemic Cohort Network (NAPKON) andwill be used to provide a comprehensive and harmonized collection of data and biomaterialfor researchers from national consortia, pharmaceutical companies and for participationin international research collaborations for the purpose of studying COVID-19 disease andfuture pandemics.

Detailed Description

The intersectoral platform is part of the National Pandemic Cohort Network (NAPKON),
which, together and in interaction with other components of the National Research Network
of University Medicine on COVID-19 (NUM), provides the essential basis for the successful
understanding and thus combating pandemics using the example of coronavirus disease 2019
(COVID-19). NAPKON represents a sustainable, integrative and comprehensive concept that
provides benefits for society as a whole in defending against and coping with pandemics,
especially at the level of public health care, in hospital and patient management and
from the individual patient's perspective.

The intersectoral platform records data and biomaterial of severe acute respiratory
syndrome coronavirus type 2 (SARS-CoV-2)-infected patients through a network of
university clinics, hospitals at all levels of care, general practitioners and specialist
practices with appropriate study experience and infrastructure. The longitudinal
phenotyping programme tracks patients for up to one year and collects detailed and
harmonized clinical data as well as biomaterial. Follow-up data is enriched by
patient-reported outcomes (PROM) and recruitment is intensified by focusing on hot-spot
regions. Mobile study teams are used to reach, among others, long-term care and
rehabilitation facilities, thus mapping all structural elements of the German care
network.

The primary aim of the intersectoral platform is to provide a comprehensive and
harmonized collection of data and biomaterial for researchers from national consortia,
pharmaceutical companies and for participation in international research collaborations
for the purpose of studying COVID-19 disease and future pandemics.

Unknown status
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)

Other: Observational of different courses of SARS-CoV-2 infection in different phases (acute vs. post-acute) and settings

Observatory Cohorts focusing (I) on subjects after SARS-CoV-2 infection that are
recruited from the general population (POP), and on subjects with acute SARS-CoV-2
infections recruited (II) in university hospital high-care settings or (III) general
health care.

Eligibility Criteria

Inclusion Criteria:

1. Age ≥18 years

2. Compliance with the case definition (a-c):

1. Polymerase chain reaction (PCR) or rapid test diagnosis from nasopharynx,
bronchoalveolar lavage, oropharynx, stool and/or blood

2. or a combination of:

- negative molecular detection of SARS-CoV-2 AND

- characteristic radiological findings AND

- respiratory tract infection AND

- absence of a more likely cause of disease, in particular other chronic
lung diseases AND

- Negative test for influenza

3. or (control group) a combination of:

- negative molecular detection of SARS-CoV-2 AND

- respiratory tract infection AND

- absence of a more likely cause of disease, in particular other chronic
lung diseases AND

- attempt of pathogen identification from respiratory material with at least
culture and influenza test

3. The baseline visit needs to be performed a maximum of 7 days (168h) after sampling
and 4 days (96h) after the case definition is available.

4. Signed informed consent

Exclusion Criteria:

1. Age <18 years

2. Paediatric patients will not be included at the beginning of the study (amendment in
preparation).

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
Germany
Locations

RWTH Aachen
Aachen, Germany

University Hospital Augsburg
Augsburg, Germany

Charité Berlin
Berlin, Germany

Klinikum Bielefeld
Bielefeld, Germany

University Hospital Ruhr-University Bochum
Bochum, Germany

University Hospital Bonn
Bonn, Germany

University Hospital Cologne
Cologne, Germany

University Hospital Carl Gustav Carus Dresden
Dresden, Germany

University Hospital Dusseldorf
Dusseldorf, Germany

University Hospital Erlangen
Erlangen, Germany

University Hospital Essen
Essen, Germany

Johann Wolfgang Goethe University
Frankfurt am Main, Germany

University Hospital Freiburg
Freiburg, Germany

University Hospital Greifswald
Greifswald, Germany

University Hospital Göttingen
Göttingen, Germany

University Hospital Halle
Halle/Saale, Germany

University Hospital Hamburg-Eppendorf
Hamburg, Germany

University Hospital MMH Hannover
Hannover, Germany

University Hospital Heidelberg
Heidelberg, Germany

University Hospital UKS Homburg
Homburg, Germany

University Hospital Jena
Jena, Germany

University Hospital UKSH Schleswig-Holstein
Kiel, Germany

University Hospital Leipzig
Leipzig, Germany

University Hospital UKSH Schleswig-Holstein
Lübeck, Germany

University Hospital Mannheim
Mannheim, Germany

University Hospital Giessen/Marburg
Marburg, Germany

University Hospital LMU Munich
Munich, Germany

University Hospital TUM Munich
Munich, Germany

University Hospital Münster
Münster, Germany

Klinikum Oldenburg
Oldenburg, Germany

University Hospital Regensburg
Regensburg, Germany

University Hospital Tübingen
Tübingen, Germany

University Hospital Ulm
Ulm, Germany

University Hospital Würzburg
Würzburg, Germany

Contacts

Jörg J Vehreschild, Prof.
+49 221 478-88794
Janne.Vehreschild@kgu.de

Jörg J Vehreschild, Prof., Principal Investigator
Johann Wolfgang Goethe-Universität Frankfurt am Main

Nationwide Network of University Medicine (NUM) on Covid-19
NCT Number
Keywords
SARS-CoV-2
Covid-19
Coronavirus
cohort
NAPKON
NAPKON-SÜP
Quality of Life
longterm morbidity
MeSH Terms
Coronavirus Infections
Severe Acute Respiratory Syndrome