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A total of 80 study subjects (39 AJG522, 41 PEG + E) were registered and randomized, 75 of whom completed the study preparations (38 AJG522, 37 PEG + E).
Thus it was recommended that the study preparations and communication with the participating institutions start early to enable a timely start of the survey, that institutions select their clients in close cooperation with the research organizations, and that more clarity is needed about the sample sizes and the minimal numbers of eligible clients.
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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).
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