Table 1.
Simulants’ study | N | Method | Outcome | Conclusion |
---|---|---|---|---|
Short-acting stimulants | ||||
MPH* (Spencer et al 1995) | 23 | Duble-blind crossover study | ADHD symptoms ↓ (78%) | MPH is significantly more effective than placebo |
MPH (Spencer et al 2005) | 146 | Duble-blind randomized study | ADHD symptoms ↓ (76%) No serious CV adverse events | MPH is significantly more effective than placebo Good tolerability |
Long-acting stimulants | ||||
Controlled release MPH/Biphentin/ (Jain et al 2007) | 39 | Double-blind placebo-controlled crossover study | ADHD symptoms ↓ Weight loss | Successful in symptoms control Well tolerated |
OROS-MPH/Concerta/(Fallu et al 2006) | 32 | Uncontrolled, open label study | ADHD symptoms ↓ Functional improvements (Sheehan scale) | Successful control of symptoms Less functional disability |
OROS-MPH/Concerta/ (Biederman et al 2006) | 141 | Double-blind, randomized, placebo controlled study | ADHD symptoms ↓ ↑Systolic and diastolic blood pressure and heart rate | Successful control of symptoms Concerns about CV tolerability |
OROS-MPH/Concerta/ (Reimherr et al 2007) | 47 | Double-blind, placebo-controlled, crossover study | ADHD symptoms ↓ (41%–42% symptoms reduction) | Less remarkable improvement than in other comparable studies |
Mixed amphetamine salts XR/Adderall XR/(Biederman et al 2005) | 223 | Double-blind, placebo-controlled study | ADHD symptoms ↓ (sustained improvement up to 24 months) Good tolerance | Sustained symptomatic impovement Well tolerated |
MPH – methylphenidate