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. 2016 May 5;12:1085–1101. doi: 10.2147/NDT.S94158

Table S4.

CGI-S normal/borderline ill (CGI-S score of 1 or 2) and mildly ill or greater (CGI-S score of ≥3) at baseline and end point by treatment for prior MPH or stimulant-naïve subgroups (LOCF; full-analysis set)

CGI-S RCT
RWS
Placebo (n=111) GXR (n=114) ATX (n=112) GXR (n=503)

Prior MPH Stimulant-naïve Prior MPH Stimulant-naïve Prior MPH Stimulant-naïve Prior MPH Stimulant-naïve
Baseline
Number of participants 48 55 46 61 48 58 224 207
Normal/borderline, n (%) 0 0 0 0 0 0 0 0
Mildly ill or greater, n (%) 48 (100) 55 (100) 46 (100) 61 (100) 48 (100) 58 (100) 224 (100) 207 (100)
End point
Number of participants 48 55 45 60 48 58 222 206
Normal/borderline, n (%) 9 (18.8) 15 (27.3) 16 (35.6) 24 (40.0) 7 (14.6) 20 (34.5) 152 (68.5) 146 (70.9)
Mildly ill or greater, n (%) 39 (81.3) 40 (72.7) 29 (64.4) 36 (60.0) 41 (85.4) 38 (65.5) 70 (31.5) 60 (29.1)
Difference in % normal/borderline from placebo (95% CI; P-value) 16.8 (−1.0 to 34.6; P=0.070) 12.7 (−4.4 to 29.8; P=0.073) −4.2 (−19.1 to 10.7; P=0.516) 7.2 (−9.8 to 24.2; P=0.242)

Note: P-values based on Cochran–Mantel–Haenszel statistic comparing the treatment groups, with country and age-group included as stratification factors.

Abbreviations: ATX, atomoxetine; CGI-S, Clinical Global Impression – Severity scale; CI, confidence interval; GXR, guanfacine extended release; LOCF, last observation carried forward; MPH, methylphenidate; RCT, randomized controlled trial; RWS, randomized-withdrawal study.