Exemplos de uso de Final sample size em Inglês e suas traduções para o Português
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The final sample size was of 1,273 patients.
A loss percentage of 35% was adopted,so the final sample size was increased to 153 subjects.
Final sample size obtained was comprised of 117 individuals in CS and 155 in RP.
The power for the final sample size was calculated at 70.
Because of possible losses or refusals to participate,another 20% was added, and the final sample size was 1,800.
We decided to establish a final sample size between 320 to 480 patients.
A final sample size of 300 women was achieved, with a 17% safety margin.
After exclusion criteria, a final sample size of 307 students 146 boys 11.9±.
The final sample size was 1,059 interviewees statistically representative.
Adding 10% for possible losses, a final sample size of 1,324 children was arrived at.
The final sample size ranged from 1918 to 4019, and the mean age of participants ranged from 51 to 54 years.
By admitting a non-response rate of 20%, the final sample size was n 120 for CS and n 174 for RP.
The final sample size in this phase comprised 341 cases, 82.9% of the study sample(341/411) Table 1.
Considering possible sample loss of 15%, the final sample size was estimated in 39 patients.
Final sample size was estimated as a minimum of 12 adolescents per group and, therefore, at least 48 adolescents were required.
To obtain the estimate with 95% confidence interval andsample error of 10%, final sample size was 568 individuals.
Based on this need, the final sample size was defined as 1,067 patients, considered sufficient for readings with such segmentations.
Considering the possible information loss,we added approximately 30% to the final sample size and recruited 201 mothers.
The final sample size included a 10% increase to compensate for eventual losses and refusals, 15% for confounders and a design effect of around 1.3.
About 20% was added to that number to compensate for possible losses, and the final sample size was 86 infants.
The final sample size was 2,016 individuals, with an added 10% to cover refusals and 20% to control for confounding factors in the multivariate analysis.
Two of the patients who agreed to participate in the study were excluded as they had an ABI>1.40 1.1% resulting in a final sample size of 176.
The calculation resulted in 235 elderly,however, the final sample size was 286, since some elderly requested to participate as he/she saw another elderly taking part in the research.
Optical reading reduced possible information bias resulting from the transcription to negligible levels, and the final sample size corresponded to a statistical power of 97.
After the addition of a 5% safety margin, the final sample size was 557 children, and 585 children were evaluated after they submitted an informed consent form signed by their parents or guardians.
Assuming that there is a relative homogeneity of births between the months of the year, the final sample size was obtained by dividing the total sample by 12 months.
The final sample size by chance was precisely 500 patients who had lateral cephalograms prior to treatment about 8.5 years old and prior to Phase II treatment about 12.5 years of age.
Table 1 describes the success rates of the interviews,the percentage of refusals and the final sample size of each of the surveys conducted from 2006 to 2009.
However, because of the considerably large final sample size greater than needed for the representative population, it is believed that this loss of participants has reduced the information bias that could influence the results.
During processing, records with no data from the woman orno new-born medical records were excluded and the final sample size accounted for 23,894 postnatal women Table 1.