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The maximum doses of these studies were decided based on the RP2Ds for tivantinib monotherapy in a previous Japanese phase I study (ARQ 197-0701; Yamamoto et al, 2013).
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A final selection of included studies was decided by discussion with the whole team.
The timing of HUS studies was decided by the neonatologist attending the service.
Where discrepancies emerged (n = 14 papers) the inclusion/exclusion of these studies was decided by consensus.
The final decision to include studies was decided by consensus with the third reviewer resolving any discrepancies.
In step 1, the exclusion of irrelevant studies was decided by considering only the title and abstract; when the abstract of a particular article was not available, the article was selected for evaluation in step 2, except when the title unequivocally presented information for exclusion (e.g. case report, studies of risk factors in a specified population).
Time consistently emerged as an important factor when the men in our study were deciding whether they could fix the problem themselves or whether they needed to seek professional help.
Fields of study are decided in consultation with sponsoring professor.
Once the design and measuring instruments for a study are decided, a sample size must be chosen.
The size of the study was decided based on considerations on the number of predictors to be tested in the predictive model.
The size of the study was decided from the following power considerations.
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CEO of Professional Science Editing for Scientists @ prosciediting.com