Study of Changes in Total Cholesterol Levels as a Function of Consuming a Supplement Designed to Improve Cardiovascular Health

NCT ID: NCT01890889

Last Updated: 2013-11-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-07-31

Study Completion Date

2013-12-31

Brief Summary

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The purpose of this study is to evaluate the effectiveness of a food-source nutrient containing bitter orange by comparing changes 45 blood chemistries and self-reported quality of life.

Detailed Description

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To evaluate the safety and efficacy of a food-source nutrient by comparing changes in total cholesterol levels, 44 other blood chemistries, and self-reported quality of life as a function of consuming two different functional-food supplements versus a placebo in a 60-day study.

Upon completion of the pre-study screening, and after having received an explanation of the requirements, risks and benefits, and completing the informed consent interview with the research coordinator, subjects will execute a written informed consent. Subjects will be randomly assigned to one of three study groups.

Relevant Background Information.

A factor leading to development of vascular disease, a leading cause of death in industrialized nations, is elevated serum cholesterol. It is estimated that 19% of Americans between the ages of 20 and 74 years of age have high serum cholesterol. However, in an analysis of 10,000 test results in our database from subjects similar to those who are likely to participate in this study, we found 37% of subjects had TC scores between 200 and 250 and 10.3% above 250.

The most prevalent form of vascular disease is arteriosclerosis, a condition associated with the thickening and hardening of the arterial wall. The regulation of whole-body cholesterol homeostasis involves the regulation of intestinal cholesterol absorption, cellular cholesterol trafficking, a modulation of cholesterol biosynthesis, bile acid biosynthesis, steroid biosynthesis and the catabolism of the cholesterol-containing plasma lipoproteins. Regulation of intestinal cholesterol absorption has proven to be an effective means by which to regulate serum cholesterol levels.

Ad-Chol-Pre (ACP) is a functional food ingredient designed to inhibit cholesterol absorption. ACP is a freeze dried defatted egg powder containing specific Anti-NPCIL1 (Niemann-Pick C1-like 1) IgY. NPC1L1 is known as a biological target of the cholesterol-uptake inhibitor, Ezetimibe. In previous unpublished pilot studies examining the safety and efficacy of ACP include:

* ACP was shown to produce a statistically inhibition of \[3H\]-Cholesterol absorption from 50 ug/ml (P\<0.05) in NPC1L1 over-expressing HepG2 cell lines as compared to an inhibition of 10ug/ml with Ezetimibe alone.
* I preliminary unpublished animal studies, ACP was shown to significantly inhibit radiolabelled cholesterol. ACP was found to significantly lower total cholesterol (38% \~56%) and LDL cholesterol (46\~57%) in bloods from animals fed who had been fed a high fat diet for 6 weeks.

Conditions

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Cholesterol Hyperlipidemia Hypercholesteremia

Keywords

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Total Cholesterol LDL

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Ad-Chol-Pre

A functional food ingredient designed to inhibit cholesterol absorption. ACP is a freeze dried defatted egg powder containing specific Anti-NPCIL1 (Niemann-Pick C1-like 1) IgY. NPC1L1 is known as a biological target of the cholesterol-uptake inhibitor, Ezetimibe.

Group Type ACTIVE_COMPARATOR

Ad-Chol-Pre

Intervention Type DIETARY_SUPPLEMENT

Half-dose Ad-Chol-Pre

A half-dose of the active comparator in arm one is administered. A functional food ingredient designed to inhibit cholesterol absorption. ACP is a freeze dried defatted egg powder containing specific Anti-NPCIL1 (Niemann-Pick C1-like 1) IgY. NPC1L1 is known as a biological target of the cholesterol-uptake inhibitor, Ezetimibe.

Group Type ACTIVE_COMPARATOR

Half-dose Ad-Chol-Pre

Intervention Type DIETARY_SUPPLEMENT

Capsule containing inactive component of defatted egg yolk

Placebo capsule is filled with defat egg yolk only without specific IgY which is anti-NPC1L1 IgY, designed to look and taste the same as the active product capsule, but does not contain the active component.

Group Type PLACEBO_COMPARATOR

Defatted egg yolk without the active ingredient of the other two interventions

Intervention Type OTHER

Interventions

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Ad-Chol-Pre

Intervention Type DIETARY_SUPPLEMENT

Half-dose Ad-Chol-Pre

Intervention Type DIETARY_SUPPLEMENT

Defatted egg yolk without the active ingredient of the other two interventions

Intervention Type OTHER

Other Intervention Names

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Anti-NPC1L1 IgY Ezetimibe Ad-Chol-Pre Anti-NPC1L1 IgY Ezetimibe Capsule manufactured to mimic the Ad-Chol-Pre capsule, only not containing the active component.

Eligibility Criteria

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Inclusion Criteria

* be an English-speaking male or female at least 18 years of age;
* have a total cholesterol level between 200 mg/dL and 250mg/dL
* have a LDL level between 100 mg/dL and 160 mg/dL
* not have allergic reactions to eggs or egg products
* not have consumed cholesterol-lowering drugs within 2 months of starting the study
* agree to follow the requirements of the study as set forth in this Informed Consent
* agree to withdraw from the study if becoming pregnant during the study.

Exclusion Criteria

* do not speak English;
* are under 18 years of age;
* have a total cholesterol level below 200 mg/dL or above 250 mg/dL
* have a LDL level below 100 mg/dL or above 160 mg/dL
* have allergic reactions to eggs or egg products
* have consumed cholesterol-lowering drugs within 2 months of starting the study
* are pregnant or nursing;
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Integrative Health Technologies, Inc.

NETWORK

Sponsor Role lead

Responsible Party

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Gilbert R Kaats

Dr. Gilbert R. Kaats, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Gilbert R Kaats, PhD FACN

Role: PRINCIPAL_INVESTIGATOR

Integrative Health Technologies, Inc.

Harry G Preuss, MD MACN

Role: STUDY_CHAIR

Georgetown University Medical Center, Dept of Biochemistry, Medicine and Pathology

Sidney J Stohs, PhD

Role: STUDY_DIRECTOR

Dean Emeritus, Creighton University Health Sciences Center

Locations

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Integrative Health Technologies

San Antonio, Texas, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Patricia L Keith

Role: CONTACT

Phone: 210-824-4200

Email: [email protected]

Facility Contacts

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Patricia l Keith, BBA

Role: primary

Mike E Gale, BS

Role: backup

Other Identifiers

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065

Identifier Type: -

Identifier Source: org_study_id