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Table 3 Subjects allocation per trial arm and subgroup and baseline characteristics

From: A yeast fermentate improves gastrointestinal discomfort and constipation by modulation of the gut microbiome: results from a randomized double-blind placebo-controlled pilot trial

 

Gender

Age

BMI (kg/m2)

GI symp. DTS a

Cohort

Treatment

n

Males (n)

Females (n)

Range

Median

Range

Median

Mean (± SEM)

Total cohort (n = 80)

EpiCor

40

7

33

20–69

50

18–33

24

7.20 ± 0.56

Placebo

40

6

34

21–65

45

18–35

24

6.56 ± 0.46

Severe (n = 55)

EpiCor

28

5

23

24–66

48

18–33

24

8.68 ± 0.60

Placebo

27

3

24

21–65

44

18–33

24

8.08 ± 0.42

Moderate (n = 25)

EpiCor

12

2

10

20–69

57

19–33

23

3.74 ± 0.31

Placebo

13

3

10

23–63

52

20–35

22

3.41 ± 0.32

  1. Legend: BMI, body mass index; GI, gastrointestinal
  2. aAverage of daily total scores (DTS) obtained after 2-week run-in on GI symptoms. This score was used to allocate subjects within the two subgroups (severe: GI symptoms ≥ 5 and moderate: GI symptoms <5)