Follow-up evaluations for Ama and placebo group

Baseline15 days30 daysBefore withdrawal 60–240 days1 week after withdrawal1 month after withdrawal
The patients who withdrew because of side effects other than dyskinesia, (shown in the figure) are omitted from calculations. (Ama, n = 17; placebo, n = 18)
Values are mean (SD).
AMA
“On” time (hours) 8.9 (2.4)9.6 (2.1)9.9 (1.9)9.0 (2.3)9.4 (2.0)9.1 (2.3)
“Off” time (hours) 6.4 (2.9)5.6 (2.5)4.8 (2.0)6.1 (2.4)6.2 (2.1)6.9 (2.3)
UPDRS I–III 52.9 (8.5)48.1 (7.8)47.2 (7.7)49.7 (7.9)51.1 (8.8)51.5 (9.2)
UPDRS IV 32–34 6.7 (2.8)2.0 (1.1)2.3 (1.0)6.1 (2.8)7.0 (2.9)6.8 (2.9)
IGA reduction % 1001000058
unchanged % 0063535
increase % 0094657
DRS 19.6 (1.2)10.5 (1.3)10.3 (1.6)18.4 (1.5)22.2 (3.4)20.4 (1.4)
PLACEBO
“On” time (hours) 9.1 (2.1)9.2 (2.0)9.1 (2.2)9.0 (1.9)9.0 (2.1)9.0 (1.8)
“Off” time (hours) 6.2 (2.4)6.1 (2.1)6.2 (2.2)6.3 (2.1)6.3 (2.3)6.3 (2.2)
UPDRS I–III 52.7 (8.2)52.5 (8.3)52.7 (8.2)52.8 (8.1)52.8 (8.2)52.4 (8.0)
UPDRS IV 32–34 6.6 (2.6)6.1 (2.4)6.4 (2.6)6.7 (2.6)6.8 (2.4)6.8 (2.3)
IGA reduction % 11110028
unchanged % 8361617261
increase % 628392811
DRS 20.4 (1.9)20.2 (1.6)20.0 (1.6)20.2 (1.5)20.4 (1.7)20.9 (1.7)