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. 2012 Sep 3;17(9):10503–10539. doi: 10.3390/molecules170910503

Table 1.

Natural bioactive compounds in clinical trials.

Bioactive Compound/Intervention Study design Memory test Result/Activity Ref.
Galantamine Patients with Mild to moderate AD, R, DB, PC (3 months/n = 386) CIBIC-plus and ADAS-cog Improved cognitive function and basic activities of normal living than placebo in AD patients. [13]
Galantamine (8, 16 & 24 mg/day) Patients with Mild to moderate AD, R, DB, PC, M (5-month) ADAS-cog and CIBIC-plus Benefits the cognitive, functional, and behavioral symptoms of AD as compared with placebo. [14]
Galantamine (24 or 32 mg/day) Patients with Mild to moderate AD, M, DB, (6-month/n = 636) ADAS-cog and CIBIC-plus Improved cognition and global function, better outcome on CIBIC-plus and ADAS-cog. [15]
Galantamine (24 or 32 mg) Patients with Mild to moderate AD, R, DB, PC blind, parallel group, trial (6-month/n = 653) ADAS-cog Better scores on the disability assessment for dementia, slowed the decline of functional ability as well as cognition in subjects with mild to moderate AD as compared with placebo. [16]
Galantamine (24 mg/day) Patients with Vascular dementia, M, DB, (n = 592) ADAS-cog and CIBIC-plus Therapeutic effect on all key areas of cognitive and non-cognitive abilities with improved activities of daily living and behavioral symptoms were also significantly improved in dementia patients. [17]
Galantamine (24 mg/day) Patient with severe AD, R, DB, PC, blind (n = 207) SIB and MDS-ADL Improvement in memory, praxis, and visuospatial ability. [18]
Huperzine A (0.2 mg twice daily) R, DB, PC with AD (n = 28) MMSE, ADL, HDS and WMI Improved memory test scores over the individuals receiving the placebo. [20]
Huperzine A (0.4 mg daily) Subjects with benign vascular dementia, and AD (n = 80) MQ test Significant improvement in MQ test as compared to control group. [21]
Huperzine Alpha (400 μg/day) Subjects with diagnosis of possible or probable AD (n = 100/12 weeks) ADL &ADAS-Cog Remarkably improves the cognition, behavior, ADL, and mood of AD patients as assessed by ADAS-Cog. [22]
Huperzine A (200 & 400 μg; twice daily) Patients with mild to moderate AD, M, R (16 weeks/n = 210) ADAS-Cog Huperzine A 400 μg and not at 200 μg has cognitive effect in patients with mild to moderate AD. [23]
Huperzine A (0.1 mg twice daily) Patients with mild to moderate VaD, R, DB ,PC (12 weeks/n = 78) CDR, MMSE, and ADL Huperzine A showed significant improvement in cognitive functions of all test. [24]
Bacognize® (300mg; twice daily) Patients with AD, R, DB, PC and M (6 months) MMSE Improvement in attention, language, reading, writing & comprehension. [25]
Bacopa monniera Healthy individuals, DB, PC (n = 46) Well-validated neuropsychological tests Significant improvement in information processing and memory consolidation, & in state anxiety. [26]
Bacopa monniera (2 × 150 mg) Healthy individuals, DB, PC (90 days/n = 127) Neuropsychological testing using the Cognitive Drug Research cognitive assessment system Improves partial working memory and reduced number of false positives in the rapid visual information processing task. [27]
Bacopa monniera (300 mg) 65 or older year individuals, R, DB, PC (12weeks/n = 54) AVLT, DAT, and WAIS Enhances AVLT delayed word recall memory scores and also improves ability to ignore irrelevant information as assessed by Stroop test. [28]
BT-11 (extracted from roots of Polygala tenuifolia) Healthy elderly individuals, R, DB, PC (n = 28) CERAD and MMSE Treatment by BT-11, increased CERAD scores, word list recognition, constructional recall and praxis, and modified Boston naming test. [29]
BT-11 Healthy individuals, R, DB, PC (4 weeks) K-CVLTSOPT Improvement in verbal memory and working memory. [30]
EGb 761 (240 mg) Patients with AD and multi-infarct dementia, R, DB, PC (24 weeks/n = 216) CGI and NAB Effective in Alzheimer and multi-infarct dementia. [31]
EGb 761 (240 mg/day or 160 mg/day) Patient with AD or VaD or AAMI, R, DB, PC (n = 214/24 weeks) SKT, CGI and NAI-NAA EGb 761 is not beneficial for dementia patients. [32]
EGb 761 (Ginkgo extract - 180 mg/day) Aged subjects with no history of significant neurocognitive dysfunction (6 weeks) Stroop Color and Word Test color-naming task Significantly showed improvement on a task assessing speed of processing abilities. [33]
Standardized extract of Ginkgo biloba (GK501) & Standardized extract of Panax ginseng (G115) (60 mg - Capsule) Healthy individuals, DB, PC (14 week/n = 256) Tests for attention and memory from the Cognitive Drug Research computerized cognitive assessment system Significantly to improve an Index of Memory Quality, memory, including long-term and working memory. [34]
Capsulated aqueous extract of C. asiatica (250, 500, and 750 mg) Healthy individuals, R, DB, PC (2 months/n = 28) Computer assisted technique Cognitive enhancing effect observed. [35]
Ginseng (400 mg) Healthy young volunteer, R, DB, PC, balanced, cross-over (n = 20) CDR two serial subtraction mental arithmetic tasks Improvement in the speed and accuracy of memory and attentional tasks. [36]
Panax ginseng extract (G115) (400 mg) Healthy middle aged individuals, DB, PC balanced trail (n = 30) Cognitive and mood performance test Improvement speed of attention and tasks associated with episodic memory performance. [37]
Cereboost(P. quinquefolius standardized to 10.65% ginsenosides) Healthy young volunteer, R, DB, PC, crossover trial (n = 32) Parameters for mood and neurocognitive effect Improvement working memory performance, reaction time accuracy and calmness. [38]
G115 (200 mg & 400 mg) Healthy young volunteer, R, DB, PC, crossover trail (n = 30) COGNITIVE BATTERY (Bond-Lader visual analogue scales, Computerised Corsi block tapping task, N-back task and Random number generation task Modulation of cognitive function and mood. [39]
HT100 (proprietary North American ginseng extract) Individuals with schizophrenia, DB, PC (4 weeks/n = 64) Letter-Number Span Test and Visual Pattern Test Significant improvement in visual working memory. [40]
LGNC-07 (combination of green tea extract and L-Theanine/1,680 mg) MCI subjects, DB, PC (16 weeks/n = 91) Rey–Kim memory test and Stroop color-word test Significant improvement in selective attention, cognitive alertness, memory and verbal reading. [41]
Green Tea Cross-sectional trial (n = 1003) MMSE Higher consumption of green tea lowers prevalence of cognitive impairment. [42]
Total Tea Cross-sectional and longitudinal (n = 2501) MMSE Total tea consumption lowers risk of cognitive impairment and cognitive decline. [43]
Total Tea Cross-sectional trial (n = 716) MMSE Total tea consumption improves global cognition, memory, executive function, and information processing speed. [44]
Salvia officinalis extract (60 drops/day) Patients with mild to moderate AD, DB, R, PC (n = 424 months) ADAS-cog & CDR Improvement in cognitive functions. [45]
Extract of Salvia officinalis (167, 333, 666 and 1332 mg) Patients with mild to moderate AD, DB, R, PC (n = 20) CDR Enhancement of secondary memory performance. [46]
S. officinalis aroma Healthy individuals, SB, one factor, independent group trial (n = 135) CDR & Bond-Lader mood scale Significantly increases the alertness in mood and quality of memory. [47]
S. lavandulaefolia (25 and 50 μL) Healthy individuals, PC, DB, balanced, crossover trail (n = 24) CDR & Bond-Lader mood scale Improvement on the speed of memory and secondary memory. [48]
Tofu Honolulu-Asia Aging Study (n = 3734) All task included in Cognitive abilities screening instrument(CASI) Higher midlife tofu consumption was independently associated with indicators of cognitive impairment and brain atrophy in late life. [49]
Dietary phytoestrogens Cross-sectional study (n = 301) Functions like, memory, processing capacity, speed and executive function High lignan intake improves capacity, speed and executive function. [50]

DB = Double blind; SB = Single blind; PC = Placebo controlled; R = Randomized; M = Multicentre; ADAS-Cog 11 = 11-item Alzheimer’s disease Assessment Scale-Cognitive subscale; CASI = Cognitive abilities screening instrument; MMSE = Mini-mental state examination; CDR =Clinical dementia rating; ADL = Activities of daily living; CERAD = Consortium to Establish a Registry for AD Assessment Packet; K-CVLT = Korean version of the California Verbal Learning Test; SOPT = Self-Ordered Pointing Test; Auditory Verbal Learning Test (AVLT); DAT = Divided Attention Task; WAIS = Wechsler Adult Intelligence Scale; AVLT = Auditory Verbal Learning Test; Nurnberger NAB = Alters-Beobachtungsskala; SKT = Syndrome Kurz Test; CGI = Clinical Global Impression; NAI-NAA = Nuremberg Gerontopsychological Rating Scale for Activities of Daily Living; WJCAT III = Woodcock-Johnson Cognitive Abilities Test III.