Table 9.
Population: Recent
ischaemic stroke Intervention: Actovegin daily intravenous then oral Comparator: placebo | |||
Outcome | No of participants | Difference in mean change from baseline at 6 months | Quality of evidence (GRADE) |
Cognition (ADAS-Cog) | One trial, n = 196 (actogevin) vs 202 (placebo) | Mean change from baseline: −2.3 (−3.9, −0.7); p = 0.005 |
Very low a |
Adverse events | One trial, n = 250 (actogevin) vs 253 (placebo) | % Discontinuing due to
AE actovegin: 8.4%; placebo: 6.6% |
Very low b |
BPSD | No data | ||
Caregiver strain | No data |
aDowngraded due to imprecision; publication bias and inconsistency.
bDowngraded due to serious imprecision; publication bias and inconsistency.