Krüger, Lisa J.
Klein, Julian A. F.
Tobian, Frank
Gaeddert, Mary
Lainati, Federica
Klemm, Sarah
Schnitzler, Paul
Bartenschlager, Ralf
Cerikan, Berati
Neufeldt, Christopher J.
Nikolai, Olga
Lindner, Andreas K.
Mockenhaupt, Frank P.
Seybold, Joachim
Jones, Terry C.
Corman, Victor M.
Pollock, Nira R.
Knorr, Britta
Welker, Andreas
de Vos, Margaretha
Sacks, Jilian A.
Denkinger, Claudia M. http://orcid.org/0000-0002-7216-7067
Assaad, K.
Fuhs, A.
Harter, C.
Schulze, C.
Schmitt, G.
Klemmer, Anja
Müller, Rico
Fink, Martina
Fougereau, Mathilde
Schirmer, Maximilian
Small, Annika
Meinlschmidt, Matthias
Dürr, Valerie
Schuckert, Alina
Backes, Ann-Kathrin
Steinke, Salome
Ellinghaus, Henrik
Abutaima, Loai
Kollatzsch, Mandy
Wintel, Mia
Kausch, Franka
Hommes, Franziska
Bölke, Alisa
Bernhard, Julian
Hülso, Claudia
Linzbach, Elisabeth
Rössig, Heike
Gertler, Maximilian
Burock, Susen
von dem Busche, Katja
Patberg, Stephanie
,
Clinical trials referenced in this document:
Documents that mention this clinical trial
Evaluation of accuracy, exclusivity, limit-of-detection and ease-of-use of LumiraDx™: An antigen-detecting point-of-care device for SARS-CoV-2
https://doi.org/10.1007/s15010-021-01681-y
Head-to-head performance comparison of self-collected nasal versus professional-collected nasopharyngeal swab for a WHO-listed SARS-CoV-2 antigen-detecting rapid diagnostic test
https://doi.org/10.1007/s00430-021-00710-9
Funding for this research was provided by:
Ministry of Science, Research and Arts of the State of Baden-Wuerttemberg
University Hospital Heidelberg
University Hospital Charité - Universitätsmedizin Berlin
UK Department of International Development (300341-102)
World Health Organization
Unitaid (2019-32-FIND MDR)
NIAID-NIH CEIRS (HHSN272201400008C)
Universitätsklinikum Heidelberg
Article History
Received: 30 April 2021
Accepted: 25 July 2021
First Online: 12 August 2021
Declarations
:
: The authors declare no conflict of interest.
: The study protocol was approved in March 2020 by the ethical review committee at the Heidelberg University Hospital for the two study sites Heidelberg and Berlin in Germany (Registration number S-180/2020). All participants provided written informed consent prior to inclusion in the study. The study was registered in the German clinical trial registry with the registration number DRKS00021220.
: Written informed consent was obtained from all individual participants included in the study.
: Not applicable.