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The sample size for the study was determined using the sample size determination formula for comparing two population means.
The sample size for the study was determined using the World Health Organization's Sample Size Determination in Health Studies.
The minimum sample size of 385 subjects for the study was determined using the cross sectional studies with 4Zα2P(1−P)÷whereere W is the width of confidence intervals was 1%, Zα at 95% confidence interval = 1.96, with an estimate of 50% of subjects that were expected to be eligible for ART [10].
The required sample size of eligible mothers for the study was determined using the formula to estimate single population proportion.
The sample size for the study was determined using Raosoft sample size calculator (http://www.raosoft.com/samplesize.html) [ 18].
The sample size necessary for the study was determined using the tables for single-stage phase II trials based on the exact binomial distribution proposed by A'Hern (2001).
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The study size was determined using the computer software Programs for Epidemiologists (PEPI version 4.04x).
For each study, Cronbach's alpha was determined using the baseline WEMWBS data.
In the current study, an IVIVC for the four risperidone PLGA formulations was determined using two approaches.
The sample size was determined using Simon's Minimax two-stage design for phase II studies.
In the present study for a batch reaction, the adsorption dynamics were determined using the Eqs.
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