Enter Events(Failure rate) Control Group:

Enter Total number of patients in control Group:

Enter Events(Failure rate) in Test Group:

Enter Total number of patients in Test Group:

Enter Minimum clinically important difference(expected risk reduction in percent)

Enter Threshold of difference

Enter upper limit of Range of practical equivalence(ROPE):

Enter lower limit of Range of practical equivalence(ROPE):

Important References : Diamond and Kaul 2004 ,Diamond and Kaul 2009 , Pedroza2015 , Spieghalter

Bayesian Interpretation of clinical trial coded by Anupam K Singh, MD :

Frequentist Interpretation :

Weakly Informative Prior :

Enthusiastic Prior:

Skeptical Prior :