Elsokkary, M. http://orcid.org/0000-0002-1066-5888
Eldin, A. Bahaa
Abdelhafez, M.
Rateb, A.
Samy, M.
Eldorf, A.
Islam, B. A.
Raafat, T. A.
Gomaa, I. A.
Taema, M.
Mohamed, R.
Elshourbagy, M.
Tawfik, W.
Morad, A.
Mostafa, M.
Abbas, A.
Assar, T.
Hemeda, H.
Article History
Received: 14 May 2018
Accepted: 4 December 2018
First Online: 19 December 2018
Compliances with ethical standards
:
: Institutional review board (IRB) approval: the protocol was discussed by the ethical scientific committee and informed consent was taken before the participation.
: All evaluation forms, reports, laboratory specimens, and other records that leave the site would not comprise unique personal data to maintain subject confidentiality.
: The investigator made a great concern that a correct informed consent process was in place to make sure that potential research subjects were fully addressed about the nature and objectives of this clinical trial, the potential hazards and gains of study participation, and also their rights as research subjects. The investigator took the written, signed informed consent of each participant before performing any study-specific technique on the participant. The investigator retained the forms of original signed informed consents. All data and materials are available on request with an agreement for publication.
: All the authors declare no conflict of interest.