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[DOI] [PubMed] [Google Scholar] 115.Lismer A, Siklenka K, Lafleur C, Dumeaux V, Kimmins S

First, the FDA required all ENDS products to undergo a scientific review to prove that each product on the market is appropriate for the protection of public health. So far, the FDA has issued marketing orders that allow a small number of tobacco-flavored ENDS to be sold, while not making decisions on several other types of flavored ENDS

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The target sample size was 636, based on power analysis for the primary research question using G*Power, with 90% power to determine an effect size (f2) of 0.02 on our primary outcome at an alpha level of 0.05