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VIGEL
Clinical Trials

VIGEL was studied extensively in two clinical
trials.
One study was conducted on post-menopausal women who were affected
by Female Sexual Arousal Disorder (FSAD) for at least six months.
This study was designed to determine the effects of L-Arginine (one
of Vigel's main ingredients) on vaginal blood flow and sexual arousal
as well as physiological responses to erotic stimuli. It demonstrated
that the mechanism responsible for the increase in sexual arousal
was the body's enhanced production of Nitric Oxide due to the administration
of L-Arginine.
The results of another clinical study showed a significant improvement
in the Subjects' level of desire and overall sexual satisfaction.
This double-blind, placebo-controlled study included 93 women (aged
22-73) who enrolled as participants who were lacking sexual desire.
46 of these women received L-Arginine, while the other 47 received
a placebo. The participants then used a "Female Sexual Function
Index Questionnaire" to rate their level of sexual health before
starting the study, and after taking either a placebo or the L-Arginine.
After only four weeks, 62% of the active L-Arginine group reported
significantly improved satisfaction with their overall sex life, and
64% reported an improvement in their level of sexual desire. |
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