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We acknowledge the support of the nursing and medical staff for achieving this study.
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For achieving this, we aim at studying the impact of the two preparation schemes on the chemotype recognition during the docking process in a subsequent publication.
Our study introduces a framework for achieving this goal while emphasizing the importance of considering multiple periods of the annual cycle.
It is also of interest to know how the sample size calculation/allocation should be done for achieving the study objectives originally set for the two stages (separate studies).
Careful consideration is needed to determine when the inclusion of placebo recipients is highly advantageous and when it is optional for achieving the study objectives of assessing vaccine safety, tolerability and immunogenicity.
Researchers considered the dialogical method to be the most appropriate for achieving the study objectives.
Institutional Review Board approval for research involving human subjects was sought and achieved for this study and all participants signed informed consent forms.
The outcome confirms that the maximum classification accuracy (99.28%) is achieved for this study.
The maximum achieved for this study was 0.8, indicating there are additional sources of variation.
Finally, the response rate a response rate of 21% was achieved for this study, therefore the generalisability of the findings needs to be undertaken with caution.
Whilst both Kempley et al. and Abdel-Latif have reported median response times for neonatal transfers of 85 and 75 min respectively, this cannot be used as a comparison for performance achieved in this study [8, 9].
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