During the study preparation, the Standards for Reporting of Diagnostic Accuracy (STARD) initiatives were followed.
In a forced titration study, the study preparation at different doses is given to all subjects.
In this study the study preparation was given in increasing doses every week over 5 weeks.
JCC participated in the organization of the study, preparation and finalization of the manuscript.
AN assisted in planning of the study, preparation of the study protocol and participated in conducting the study.
MC, MK and TK participated in the conception and design of the study, preparation of the manuscript and practical performance.
36 Experienced continuity of care, explored by a set of questions designed during the study preparation phase.
FJW participated in the study design of the study, preparation of the tested material, performance of cell cultures, data analysis and wrote the manuscript.
The non-HDL cholesterol was essentially unchanged by the ingestion of the study preparation over the 8 weeks of the trial (Table 3).
FJC, RAC, MEN and LCS participated in the design of the study, preparation of the manuscript and performed the statistical analysis.
