Cognition Clinical Trial
Official title:
Cognitive, Emotional, Physical, and Psychosocial Effects of Three Weeks' Prospective Double-Blind Placebo Controlled Cross-Over Exposure to Panax Quinquefolius L (REMEMBER-fX), With Optional Six Months' Open Label Follow-up
The purpose of this study is to determine the efficacy and safety of REMEMBER-fX (HT1001, an extract of Panax quinquefolius) in a human sample using standard clinical neuropsychological instruments and side effects rating scales.
Panax ginseng has been used in Asia for thousands of years to improve vitality, wakefulness,
respiration, angina, nausea, attention, memory, and diminished libido. More recently, Panax
extracts have become one of the most popular commercial herbal dietary supplements in the
West as well. Unfortunately, a limited understanding of the bioactive ingredients within the
Panax extracts resulted in a wide spectrum of available products with no guidelines for
standardization. The lack of standardization undermined any legitimate attempt to validate
the claimed health benefits of the extracts. However, recent advances in the identification,
quantification, and standardization of extract components with demonstrated systemic and
neurological actions in animals have created a novel opportunity for the controlled clinical
investigation of some Panax extracts.
A significant improvement in the standardization of Panax extracts occurred approximately 20
years ago with the introduction of a 4% minimum ginsenoside content in a formulation of
Panax ginseng C V Meyer under the trademark G115 by Pharmaton in Lugano Switzerland. This
prompted a series of investigations of short-term cognitive, physical, emotional, and
psychosocial benefits from a single dose of G115. Idiosyncratic cognitive gains were
reported, but no reliable benefits were observed in physical, emotional, or psychosocial
status. Several studies have examined the cognitive, physical, emotional, and psychosocial
benefits from sustained exposure to G115, but these studies are few in number and often
failed to include standardized behavioural measures or controlled Panax extracts.
Over the past five years, refinements in high pressure liquid chromatography (HPLC) have
allowed greater precision in Panax constituent analysis, with significant implications to
the investigation of the safety and efficacy of Panax extracts in human populations. HPLC
has been used to identify and quantify several promising neuroactive ginsenosides that are
likely relevant to the human bioactive effect of Panax extracts. Most notable are the Rg1
and Rb1 ginsenosides from Panax quinquefolius L which show a number of interesting in vitro
effects on animal tissue from the central nervous system that have led to several positive
results from studies of animal learning. Most significant, however, was the introduction of
HT1001, a precisely standardized proprietary combination of Rg1 and Rb1 ginsenosides
developed by CV Technologies in Edmonton, Alberta, Canada. Each product lot of HT1001 from
CV Technologies is tested to ensure consistency of the ginsenoside composition. The
introduction of a commercial product with a precise standardized composition of Rb1 and Rg1
has created a unique opportunity for investigating the safety and efficacy of Panax
extracts.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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