[P-204]: A 5 year double blind, randomised trial on EGb 761® efficacy on the prevention of Alzheimer's dementia in patients over 70 with memory complaint. Guidage study

2005 ◽  
Vol 1 ◽  
pp. S73-S73 ◽  
Author(s):  
Bruno Vellas ◽  
Sandrine Andrieu ◽  
Pierre-Jean Ousset ◽  
Mehemed Ouzid ◽  
Hélène Mathiex-Fortunet ◽  
...  
Healthcare ◽  
2021 ◽  
Vol 9 (12) ◽  
pp. 1678
Author(s):  
Charlotte Kloft ◽  
Robert Hoerr

Following reports of bleeding upon Ginkgo intake, we assessed whether Ginkgo extract EGb 761® affects coagulation or platelet function or increases the risk of bleeding. In a double-blind, placebo-controlled trial, prothrombin time, activated partial thromboplastin time, international normalized ratio and bleeding time were measured in patients with Alzheimer’s dementia at baseline, weeks 6 and 26. A total of 513 patients were randomized to 120 mg (n = 169) or 240 mg EGb 761® (n = 170) or placebo (n = 174). No relevant changes were found for coagulation parameters and bleeding time. Numbers of bleeding-related adverse events were similar in all groups. Concomitant intake of acetylsalicylic acid was documented for 68 patients in the placebo group and 105 in the EGb 761® groups. Within these groups, the means at baseline and week 26 differed by less than 1 unit for prothrombin time and bleeding time and less than 0.1 unit for international normalized ratio. Data on warfarin treatment in nine patients each taking placebo or EGb 761® did not indicate enhancement of warfarin effects by EGb 761®. No evidence was found that EGb 761® affects hemostasis or increases the bleeding risk. No pharmacodynamic interactions with warfarin or acetylsalicylic acid were found.


2003 ◽  
Vol 13 ◽  
pp. S315
Author(s):  
W. Deberdt ◽  
P.P. De Deyn ◽  
M.M. Carrasco ◽  
C. Jeandel ◽  
D.P. Hay ◽  
...  

1990 ◽  
Vol 11 (10) ◽  
pp. 638-647 ◽  
Author(s):  
G. Rai ◽  
G. Wright ◽  
L. Scott ◽  
B. Beston ◽  
J. Rest ◽  
...  

2009 ◽  
Vol 24 (S1) ◽  
pp. 1-1
Author(s):  
A. Mowla

Objective:Recent studies suggest that cholinergic dysfunction does not provide a complete account of age-related cognitive deficits and other neuronal systems like monoaminergic hypofunction are involved. In several studies selective serotonin reuptake inhibitors demonstrated promotion in neurogenesis in the hippocampus and enhanced memory and cognition. The aim of this study is to survey the effect of serotonin augmentation on cognition and activities of daily living in patients with Alzheimer's disease.Method:The trial was designed as a 12-week randomized, placebo-controlled, double-blind study. One hundred and twenty two patients aged 55-85 years, suffering from mild to moderate alzheimer's dementia were randomly allocated in one of the three treatment group: fluoxetine plus rivastigmine, rivastigmine alone or placebo group. Efficacy measures comprised assessments of cognition, activities of daily living and global functioning. Hamilton Depression Scale also was used to assess changes in mood throughout study.Result:Fluoxetine plus rivastigmine and rivastigmine groups demonstrated improvement on measures of cognitive and memory without any significant difference; however, the former group did better in their activities of daily living and global functioning. Patients taking placebo had significant deterioration in all the efficacy measures. Patients taking rivastigmine or rivastigmine plus fluoxetine had improvements in Hamilton Depression Scale without significant differences.Conclusion:Concomitant use of selective serotonin enhancing agents and acetyl cholinesterase inhibitors can provide greater benefit in activities of daily living and global functioning in patients with cognitive impairment. Although our study is preliminary and larger double blind studies are needed to confirm the results.


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