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Trivestin,
a novel combination of plant extracts, singled out from more than
1,228 carefully screened candidate plants, was selected for its
ability to block these established inflammatory enzymes and pathways.
Because rigorous laboratory trials confirmed Trivestins proficiency
in inhibiting gene expression of compounds that cause inflammation,
pain, and joint degradation (including IL-1 Beta, COX-2, and 5-LO),
it was predicted that Trivestin would not only reduce
pain, but also preserve the integrity of joint tissue. To establish
Trivestins safety and efficacy (and mitigate the subjective
nature of pain relief) a clinical trial was designed to compare
Trivestin to both placebo and Celebrex, a recognized
standard.
With joint pain
adversely affecting more than 80 million Americans, science continues
its search for the perfect pain reliever. Materials
that have the ability to affect the IL-1 Beta inflammatory compound,
the COX-2 inflammatory enzyme, and the 5-LO inflammatory pathway
are prime targets. For example, Celebrex,®* the most popular
prescription anti-inflammatory, has been shown to selectively inhibit
the COX-2 enzyme (but not the 5-LO inflammatory pathway). Glucosamine,
a dietary supplement widely used in the treatment of joint pain,
is neither a selective COX-2 nor a selective 5-LO inhibitor (although
it may have other benefits).
30-day, head-to-head,
double-blind clinical data were evaluated to compare safety and
efficacy of Trivestin to Celebrex. Sixty (60) subjects
with confirmed osteoarthritic joint pain were divided equally into
four (4) groups: Group 1 Placebo (sugar pill); Group 2
Celebrex (200 mg per day); Group 3 Trivestin
(250 mg per day); and Group 4 Trivestin (500
mg per day). Subjects were instructed to take the prescribed capsules
in divided doses twice per day. Improvements in joint pain, mobility,
flexibility, stiffness, and ease of motion (Quality Of Life
parameters) were assessed at 30 days using the standard WOMAC**
and SF-36 (Short-Form) evaluations.
Trivestin
was shown to be twice as effective as Celebrex (Group 3: p<0.06;
Group 4: p<0.05) [over and above placebo, of course] in reducing
pain and stiffness, increasing mobility and flexibility, and improving
overall quality of life.
The ability
of Trivestin to block multiple inflammatory enzymes
and pathways (COX-2, IL-1 Beta, and 5-LO) seems to account for Trivestins
superiority over Celebrex under the conditions of this double-blind,
clinical comparative trial.
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