Hartmann, Amely http://orcid.org/0000-0001-5934-3671
Seiler, Marcus
Funding for this research was provided by:
Geistlich Company (no award number)
Article History
Received: 13 September 2019
Accepted: 27 January 2020
First Online: 3 February 2020
Ethics approval and consent to participate
: This is a clinical non-interventional monocentre study. It was performed retrospectively during the clinical routine without any further consequences for the patient. Data were anonymized and processed in accordance with the 2013 Declaration of Helsinki on medical protocol and ethics (Declaration of Taipei on Ethical Considerations regarding Health Databases and Biobanks 2016). Due to the character of the study no approval by the local ethics committee was necessary (Regulatory of the ethic committee of Rhineland-Palatinate and described in Gaus et al. [CitationRef removed]). No administrative permissions and/or licenses were acquired by the team to access the data used in the research due to the character of the study. Using a human study design, written informed consent was obtained from patients.
: Using a human study design, written informed consent was obtained from patients.
: A.H. is working at the private practice of M.S., M.S. is the creator of Yxoss CBR.