Cholesterol Lowering Clinical Trial
Official title:
Effects of a Tocotrienol-Enriched Fraction of Palm Oil and Chinese Red Yeast Rice on Serum Lipids in Hypercholesterolemic Subjects
The purpose of this study is to determine the effects of a palm-oil derived tocotrienol (TRF) supplement or Chinese red yeast rice (CRYR) individually and in combination on blood cholesterol, and particularly LDL cholesterol, in individuals who have either elevated or normal cholesterol levels. Tocotrienols are members of the vitamin E family, and are found in barley, oats, rye, coconut oil and rice bran oil, but the richest source of tocotrienols is palm oil. Certain of these tocotrienols have been shown to be effective in lowering LDL (or 'bad') cholesterol, with no adverse effects on the HDL (or 'good') cholesterol.
The current study is designed to determine whether a dietary supplement, the
tocotrienol-enriched fraction of palm oil (TRF) will enhance the effects of a botanical
supplement, Chinese Red Yeast Rice (CRYR). Originally, CRYR was sold as a dietary supplement
in the United States until 2001. Since that time, CRYR containing monacolin K which is
chemically identical to mevinolin sold as Mevacor (now off patent) has been classified as an
unapproved drug. At the present time, there are many brands of CRYR sold over the counter in
drug stores and warehouse chains in the U.S. However, none of these have the amounts of
Monacolin K found in the CRYR which was the subject of FDA action in 2001 and none have been
proven effective in lowering cholesterol. FDA monitors the levels of monacolin K in over the
counter supplements and limits the approved levels to less than 2 mg when effective doses are
between 6 and 10 mg, in this study we will use . two capsules per day where each capsule
contains 3 mg of mevinolin as Monacolin K. The capsules also contain the rice on which the
CRYR is fermented for a total mass of 600 mg per capsule or a total daily dose of 1200mg.
The study was originally designed to focus on the effects of tocotrienol, utilized with a
statin drug. However, subjects being recruited with cholesterol levels between 200 mg/dl and
240 mg/dl did not want to take a drug. This made it impossible to recruit subjects.
Therefore, the current protocol is being submitted using a CRYR from China which has known
effects on serum lipid and will be used in this study to examine whether tocotrienol by
suppressing the increase in gene expression of 3-hydroxy-3-methyl-glutaryl-CoA reductase
(HMG-CoA) reductase will further lower serum lipid compared to the CRYR alone.
This objective will be achieved by recruiting individuals with cholesterol levels within the
l range of 200 to 240 mg/dl where drug treatment is optional. After acclimation to a step 1
American Heart Association (AHA) diet, subjects will be randomized to one of four groups to
receive 1) Placebo; 2) CRYR alone; 3) TRF alone; or 4) CRYR and TRF in combination for 12
weeks. Fasting lipids including cholesterol, triglyceride, and HDL cholesterol will be
measured at baseline, 6 weeks and 12 weeks.
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Status | Clinical Trial | Phase | |
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Completed |
NCT05038436 -
Influence of Polyglucosamine L112 on Serum Surrogate Markers of Cholesterol Absorption
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N/A |