Sample size estimation in clinical trial
Every clinical trial should be planned. This plan should include the objective of trial, primary and secondary end-point, method of collecting data, sample to be included, sample size with scientific justification, method of handling data, statistical methods and assumptions. This plan is termed as...
Main Author: | Tushar Vijay Sakpal |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2010-01-01
|
Series: | Perspectives in Clinical Research |
Subjects: | |
Online Access: | http://www.picronline.org/article.asp?issn=2229-3485;year=2010;volume=1;issue=2;spage=67;epage=69;aulast=Sakpal |
Similar Items
-
Sample size considerations in research
by: Shyam Sivasamy
Published: (2023-01-01) -
Statistical Power and Effect Size in Educational and Psychological Research
by: Faisal Ahmad Abdelfattah
Published: (2011-04-01) -
Biostatistics series module 5: Determining sample size
by: Avijit Hazra, et al.
Published: (2016-01-01) -
Preeminence and prerequisites of sample size calculations in clinical trials
by: Richa Singhal, et al.
Published: (2015-01-01) -
Statistical significance or clinical significance? A researcher's dilemma for appropriate interpretation of research results
by: Hunny Sharma
Published: (2021-01-01)