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Dear all,
In estimating sample size for a study do we only depend on the primary objectives of the study without considerations to how patients are being dosed their medications. I am working on a study that will involve dosing patients depending on their conditions will that impact the sample size in any way or it will just affect the final analysis. The primary objectives is based on binary outcome "yes or no", study will be based on non-inferiority testing and we will be looking at adverse effects and tolerance as well.
I would appreciate guidance as much as possible.
thanks
Raja
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