TABLE 1.
Author | Publicati on Year |
Recruitm ent Start Year |
Fundin g |
Grou p, N |
Durati on, wks |
Sex % male |
Age rang e, years |
Medicatio n |
Outco me measur e |
Endpoi nt dose, mg/day |
Maxim um dose, mg/day |
Hig h dose SSR I |
Medicati on- Placebo Attrition differen ce |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Rynn et al.12 | 2001 | NR | Federal | 11 11 |
9 | 67 | 5–17 | Sertraline | HAMA | 50 | 50 | No | 9.1% |
Birmaher et al.17 | 2003 | 1997 | Federal | 37 1137 |
12 | 46 | 7–17 | Fluoxetine | PARS | 20 | 20 | No | 8% |
RUPP14 | 2001 | 1997 | Federal | 63 1165 |
8 | 51 | 6–17 | Fluvoxamine | PARS | 4.0±2.2b | 300 | Yes | 6% |
March et al.13 | 2007 | 2003 | Industry | 137 11148 |
16a | 44 | 8–17 | Venlafaxine ER | SASCA | 142 | 225 | N/A | 8.0% |
Rynn et al.11 | 2007 | 2000 | Industry | 157 11163 |
8 | 58 | 6–17 | Venlafaxine ER | PARS | NR | 225 | N/A | 1.6% |
Walkup et al.15 | 2008 | 2003 | Federal | 133 1176 |
12 | 53 | 7–17 | Sertraline | PARS | 133 | 200 | Yes | 1.4% |
Wagner et al.18 | 2004 | 1999 | Industry | 163 11156 |
16a | 50 | 8–17 | Paroxetine | PARS | 32.6 | 50 | Yes | 9.4% |
Strawn et al.16 | 2015 | 2010 | Industry | 135 11137 |
10 | 47 | 7–17 | Duloxetine | PARS | 53.6 | 120 | N/A | <1% |
Geller et al.71 | 2007 | 2003 | Industry | 87 1189 |
12 | 65 | 7–17 | Atomoxetine | PARS | 1.3b | 120 | N/A | 1.7% |
Note: DBPCT = double blind, placebo-controlled trial; HAM-A = Hamilton Anxiety Rating Scale; PARS = Pediatric Anxiety Rating Scale; SAS-CA = Social Anxiety Scale for Children and Adolescents; pbo = placebo; NR = not reported
This was a 16-week trial; however, 12-week data were used for the analyses described herein.
mg/kg/day, rather than mg/day.