Randomized Controlled Trial
Copyright ©The Author(s) 2020.
World J Gastroenterol. Jul 28, 2020; 26(28): 4170-4181
Published online Jul 28, 2020. doi: 10.3748/wjg.v26.i28.4170
Table 1 Baseline characteristics of study population in a full analysis set
Placebo group, n = 120BLWT group, n = 118P value
Sex, n0.8656
Male/female45/7543/75
Age in yr, mean ± SD37.78 ± 13.9637.95 ± 13.380.9256
Body height in cm,
mean ± SD166.69 ± 7.98165.46 ± 7.330.214
Body weight in kg,
mean ± SD62.93 ± 13.0561.22 ± 11.060.2765
Education background, n (%)0.9256
Illiteracy1 (0.83)1 (0.85)
Primary school5 (4.17)4 (3.39)
Middle school19 (15.83)25 (21.19)
High school19 (15.83)18 (15.25)
Junior college16 (13.33)14 (11.86)
College16 (13.33)19 (16.1)
Higher than college44 (36.67)37 (31.36)
Table 2 Baseline disease conditions in two groups, mean ± SD
Placebo group, n = 120BLWTG group, n = 118P value
Total epigastric pain score4.63 ± 0.734.61 ± 0.720.8748
VAS score of the severity of epigastric pain6.17 ± 1.146.25 ± 1.20.6257
Frequency of epigastric pain, d/wk4.14 ± 1.734.08 ± 1.670.7964
Total FD clinical score28.18 ± 9.0229.07 ± 9.330.458
FDDQL score58.91 ± 13.7857.15 ± 15.350.3518
Table 3 Analysis of clinical response for epigastric pain in a full analysis set, n (%)
Placebo group, n = 120BLWTG group, n = 118P value
Total< 0.0001
Responsive34 (28.33)101 (85.59)
Not responsive86 (71.67)17 (14.41)
Baseline VAS score, 4 ≤ VAS < 7
Responsive27( 30.34)77 (88.51)< 0.0001
Not responsive62 (69.66)10 (11.49)
Baseline VAS score, 7 ≤ VAS ≤ 10
Responsive7 (22.58)24 (77.42)< 0.0001
Not responsive24 (77.42)7 (22.58)
Table 4 Rate of abdominal pain resolution in two groups, n (%)
Placebo group, n = 120BLWTG group, n = 118P value
Resolution rate< 0.0001
Resolved18 (15)82 (69.49)
Not resolved102 (85)36 (30.51)
Table 5 Total epigastric pain score (mean ± SD) in functional dyspepsia patients in a full analysis set
Placebo group, n = 120BLWTG group, n = 118P value
Baseline4.63 ± 0.734.61 ± 0.720.8748
Week 14.43 ± 1.174.03 ± 1.280.0125
Week 23.65 ± 1.633.2 ± 1.590.0335
Week 33.67 ± 1.422.81 ± 1.46< 0.0001
Week 43.45 ± 1.482.38 ± 1.7< 0.0001
Week 53.23 ± 1.751.84 ± 1.71< 0.0001
Week 63.19 ± 1.561.32 ± 1.5< 0.0001
Table 6 Total functional dyspepsia clinical score (mean ± SD) in two groups in a full analysis set
Placebo group, n = 120BLWTG group, n = 118P value
Baseline28.18 ± 9.0229.07 ± 9.330.458
Week 223.8 ± 9.1520.53 ± 9.770.0085
Week 420.69 ± 9.9614.12 ± 8.45< 0.0001
Week 620.52 ± 9.317.76 ± 6.67< 0.0001
Table 7 Functional Digestive Disorders Quality of Life Questionnaire total score and scores of different dimensions (6-wk baseline) (mean ± SD) in a full analysis set
Placebo group, n = 120BLWTG group, n = 118P value
Total score3.93 ± 14.7820.14 ± 15.7< 0.0001
Daily activities4.72 ± 18.6119.58 ± 19.16< 0.0001
Anxiety6.42 ± 22.5125.24 ± 21.49< 0.0001
Diet11.77 ± 74.0720.51 ± 20.590.2498
Sleep1.06 ± 18.3419.1 ± 20.27< 0.0001
Discomfort4.86 ± 17.3421.46 ± 18.15< 0.0001
Coping with disease0.45 ± 17.2815.13 ± 18.72< 0.0001
Control of disease6.45 ± 23.6523.62 ± 25.25< 0.0001
Stress7.03 ± 23.518.77 ± 22.520.0003
Table 8 Use of Talcid tablets during the observation period in a full analysis set
Placebo groupBLWTG groupP value
Use rate, n (%)
Number of users29 (24.37)9 (7.63)0.0003
Number of non-users90 (75.63)109 (92.37)