Table 3.
Adverse events reported in ZISPAST trial
Ziclague® | Placebo | p-value• | |
---|---|---|---|
N = 52 | N = 52 | ||
Adverse events • | 18 (35.3%) | 22 (43.1%) | 0.55 |
Blood pressure reduction | 5 (9.8%) | 4 (7.8%) | 1.00 |
Somnolence | 7 (13.7%) | 8 (15.7%) | 1.00 |
Weakness | 1 (2.0%) | 6 (11.8%) | 0.13 |
Worsening gait | 4 (7.8%) | 4 (7.8%) | 0.72 |
Worsening falls | 1 (2.0%) | 1 (2.0%) | 0.48 |
Pain | 2 (3.9%) | 2 (3.9%) | 0.62 |
Local allergy | 2 (3.9%) | 0 (0%) | 0.48 |
Others | 5 (9.8%) | 6 (11.8%) | 1.00 |
Number of patients who experienced adverse events (%). Considered on patients who completed at least two visits of the clinical trial (N = 52)