Sample Size Estimation

Introduction: In general, sample size calculation is conducted through a pre-study power analysis. The purpose is to select an appropriate sample size in achieving a desired power for correctly detection of a pre-specified clinical meaningful difference at a given level of significance. This study/tool will provide statistical procedures for determination of sample size required not only for testing equality, but also for testing non-inferiority/superiority, equivalence (similarity) and some survival analysis and phase II clinical trials designs that are commonly employed at various phases of clinical development. As a handful tool, it is very useful for clinical scientists and biostatisticians in the pharmaceutical industry, regulatory agencies, academia, and other scientists who are related fields of clinical development.

This program helps users to determine sample sizes for a broad range of statistical techniques, including the study of means, proportions, survival analysis, phase II clinical trials and some general cases (others).

DIRECTIONS:

Means

 

Proportions

Survival Analysis

Phase II Clinical Trials

Others