Score Changes According to Each Subtype From Baseline After 12 Weeks of Administration
Score | EPS | PDS | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Sex | Time | NOVAponin | Placebo | P-value | Sex | Time | NOVAponin | Placebo | P-value | ||
GSRS | Total | 6 wk-baseline | –2.61 ± 0.30 | –0.90 ± 0.28 | < 0.001 |
Total | 6 wk-baseline | –2.52 ± 0.32 | –1.02 ± 0.33 | 0.001 |
|
12 wk-baseline | –2.72 ± 0.30 | –1.33 ± 0.27 | < 0.001 |
12 wk-baseline | –2.57 ± 0.38 | –1.02 ± 0.41 | 0.006 |
||||
Male | 6 wk-baseline | –2.00 ± 0.71 | –1.11 ± 0.62 | 0.404 | Male | 6 wk-baseline | –1.75 ± 0.77 | –1.17 ± 0.54 | 0.045 |
||
12 wk-baseline | –2.13 ± 0.64 | –1.28 ± 0.43 | 0.281 | 12 wk-baseline | –1.75 ± 0.77 | –0.61 ± 0.64 | 0.306 | ||||
Female | 6 wk-baseline | –2.70 ± 0.33 | –0.79 ± 0.27 | < 0.001 |
Female | 6 wk-baseline | –2.64 ± 0.35 | –0.94 ± 0.42 | 0.003 |
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12 wk-baseline | –2.81 ± 0.34 | –1.36 ± 0.35 | 0.003 |
12 wk-baseline | –2.70 ± 0.42 | –1.24 ± 0.53 | 0.035 |
||||
GIS | Total | 6 wk-baseline | –4.89 ± 0.33 | –2.76 ± 0.34 | < 0.001 |
Total | 6 wk-baseline | –6.33 ± 0.43 | –3.88 ± 0.54 | < 0.001 |
|
12 wk-baseline | –4.93 ± 0.35 | –3.02 ± 0.37 | < 0.001 |
12 wk-baseline | –6.97 ± 0.40 | –4.59 ± 0.49 | < 0.001 |
||||
Male | 6 wk-baseline | –3.50 ± 0.71 | –2.67 ± 0.51 | 0.364 | Male | 6 wk-baseline | –5.88 ± 0.91 | –4.61 ± 1.09 | 0.477 | ||
12 wk-baseline | –4.38 ± 0.56 | –2.89 ± 0.54 | 0.112 | 12 wk-baseline | –6.88 ± 2.53 | –4.44 ± 3.48 | 0.090 | ||||
Female | 6 wk-baseline | –5.09 ± 0.36 | –2.82 ± 0.44 | < 0.001 |
Female | 6 wk-baseline | –6.40 ± 0.47 | –3.48 ± 0.60 | < 0.001 |
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12 wk-baseline | –5.02 ± 0.39 | –3.09 ± 0.49 | 0.003 |
12 wk-baseline | –6.98 ± 0.45 | –4.67 ± 0.62 | 0.003 |
EPS, epigastric pain syndrome; PDS, postprandial distress syndrome; GSRS, gastrointestinal symptom rating scale; GIS, gastrointestinal symptom.
aP < 0.001, bP < 0.01, cP < 0.05; compared between groups: P-value for 2 sample t test or Wilcoxon rank sum test.
Data are presented as mean ± SE.