Description:

Diabetinol ™
is a patented, published, and
proprietary blend of natural, active compounds derived from citrus. This synergistic combination of active components helps support changes in plasma glucose and insulin for individuals with elevated fasting glucose.


There are several large diabetes studies that have been conducted (VADT, ACCORD, and ADVANCE). All these studies showed that the pharmaceuticals had limitations in protection against cardiovascular risk and a high percentage of subjects were not meeting either the ADA or the AACE guidelines of control. In our 6 month study subjects on oral medications were not meeting recommended guidelines at inclusion but after 6 months of supplementation with Diabetinol they were able to achieve target goals.


With “Structure Function” claims escalating at the FTC/ FDA clinical studies are increasingly more critical. The Sugar Management category has very little human clinical proof to back Nutra claims. We mostly see rat studies and sometimes in house tests at various locations. Diabetinol ™ has the credentials to make very strong claims to support the label claims you might demand.

 

Diabetinol ™

Diabetinol ™ clinically performed as an effective choice for the management of the sugar surge/insulin response in a USA based, randomized, double blind, placebo controlled,
Phase I and Phase II human clinical study.

 

Diabetinol ™
was tested in subjects with impaired fasting glucose, prediabetes and diabetes. Those that were pre diabetic (6 month study) as well those who were diabetic were on pharmaceutical medications. The two studies covered subjects in different glycemic ranges in order to see the effect of the product on a larger mixed population. The results demonstrated that it was safe and well tolerated and efficacious in both groups


Phase I:
The 3 month study results showed that there were statistically significant increases in glucose tolerance as well as statistically significant reductions in total cholesterol (13.29%) and LDL-c (23%) from baseline to end of treatment. More importantly these changes were of clinical value.

 

Phase II:
This phase demonstrated that several acceptable diabetes treatment targets were achieved in subjects on medication for type II diabetes when supplemented with Diabetinol for 6 months when compared to those given a placebo.