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. 2014 Nov 28;9:2065–2077. doi: 10.2147/CIA.S72728

Table 2.

Characteristics of included clinical trial populations

Clinical trial Duration (weeks) Diagnostic groups (number in full analysis set) Treatment groups na Dropouts (%) Age, years, mean (SD) Sex, % female Body weight, kg, mean (SD) Prior intake of antidementia drugs (n)

AD VaD Mixed
Kanowski et al33,34 24 158 47 EGb 240 mg 109 16 (14.7) 72 (10) 68 69 (13) Nonec
Placebo 107 16 (15.0) 72 (10) 71 67 (13) Nonec
Le Bars et al30,31 52b 236 73 EGb 120 mg 161 39 (24.2) 69 (10) 51 69 (14) Nonec
Placebo 166 44 (26.5) 69 (10) 56 70 (13) Nonec
Schneider et al32 26 513 EGb 240 mg 170 30 (18) 78 (7) 56 68 (14) NDd
EGb 120 mg 169 34 (20) 79 (7) 50 6 (15) NDd
Placebo 174 39 (22) 78 (7) 52 70 (13) NDd
Nikolova et al14 22 178 80 139 EGb 240 mg 203 13 (6) 69 (8) 57 72 (13) 4
Placebo 205 17 (8) 69 (8) 60 72 (14) 3
Napryeyenko et al35 22 53 181 161 EGb 240 mg 200 4 (2) 65 (8) 86 74 (12) 2
Placebo 200 5 (3) 63 (8) 82 73 (11) 0
Ihl et al36 24 121 71 212 EGb 240 mg 206 16 (8) 65 (10) 69 74 (14) 0
Placebo 204 12 (6) 65 (9) 66 74 (14) 0
Herrschaft et al13 24 208 42 152 EGb 240 mg 205 7 (3) 65 (9) 70 76 (13) 1
Placebo 205 5 (2) 65 (9) 69 73 (13) 4

Notes: –There were no patients with these diagnoses.

*

AD with cerebrovascular disease.

a

n includes all patients randomized;

b

data for week 26 analyzed and presented;

c

there were no approved antidementia drugs when these trials were conducted;

d

not determinable (ND).

Many patients had participated in double-blind, controlled clinical trials of antidementia drugs before. How many patients received an effective antidementia drug, placebo, or an ineffective investigational drug within these trials is not known.

Abbreviations: EGb, EGb 761®; AD, Alzheimer’s disease; VaD, vascular dementia; SD, standard deviation.