Back to the Top
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.
Want to post a follow-up message on this topic?
If this link does not work with your browser send a follow-up message to PharmPK@boomer.org with "Dose and sample size" as the subject
Support PharmPK by using the
Copyright 1995-2011 David W. A. Bourne (firstname.lastname@example.org)