When designing a clinical trial an appropriate justification for the sample size should be provided in the protocol. However, there are a number of settings when undertaking a pilot trial when there is no prior information to base a sample size on. For such pilot studies the recommendation is a sample size of 12 per group. The justifications for this sample size are based on rationale about feasibility; precision about the mean and variance; and regulatory considerations. The context of the justifications are that future studies will use the information from the pilot in their design
There is currently a lot of interest in pilot studies conducted in preparation for randomised contro...
Calculating the sample size is a most important determinant of statistical power of a study. A study...
Sample size is an element of research design that significantly affects the validity and clinical re...
BACKGROUND: In conducting randomized trials, formal estimations of sample size are required to ensur...
In practice, the required sample size for a two-arm randomised controlled trial cannot always be det...
BackgroundExternal pilot or feasibility studies can be used to estimate key unknown parameters to in...
Every clinical trial should be planned. This plan should include the objective of trial, primary and...
Purpose: This review aims to explain the definition and basic principle of statistical analysis and ...
Using data obtained from a pilot study, Browne (1995) proposed a procedure for estimating the sample...
Sample size justification is an important consideration when planning a clinical trial, not only for...
Background There is little published guidance as to the sample size required for a pilot or feasibi...
The calculation of the sample size needed for a clinical study is the challenge most frequently put ...
An essential part of any medical research is to decide how many subjects need to be studied. A forma...
Calculating the sample size is a most important determinant of statistical power of a study. A study...
Pilot studies are small‐scale studies conducted to gather information and provide a foundation for t...
There is currently a lot of interest in pilot studies conducted in preparation for randomised contro...
Calculating the sample size is a most important determinant of statistical power of a study. A study...
Sample size is an element of research design that significantly affects the validity and clinical re...
BACKGROUND: In conducting randomized trials, formal estimations of sample size are required to ensur...
In practice, the required sample size for a two-arm randomised controlled trial cannot always be det...
BackgroundExternal pilot or feasibility studies can be used to estimate key unknown parameters to in...
Every clinical trial should be planned. This plan should include the objective of trial, primary and...
Purpose: This review aims to explain the definition and basic principle of statistical analysis and ...
Using data obtained from a pilot study, Browne (1995) proposed a procedure for estimating the sample...
Sample size justification is an important consideration when planning a clinical trial, not only for...
Background There is little published guidance as to the sample size required for a pilot or feasibi...
The calculation of the sample size needed for a clinical study is the challenge most frequently put ...
An essential part of any medical research is to decide how many subjects need to be studied. A forma...
Calculating the sample size is a most important determinant of statistical power of a study. A study...
Pilot studies are small‐scale studies conducted to gather information and provide a foundation for t...
There is currently a lot of interest in pilot studies conducted in preparation for randomised contro...
Calculating the sample size is a most important determinant of statistical power of a study. A study...
Sample size is an element of research design that significantly affects the validity and clinical re...