Athens, GANCT07246408Now EnrollingIRB Ready

Dyslipidemia Clinical Trial in Athens, GA

Access cutting-edge dyslipidemia treatment through this clinical trial at a research site in Athens. Study-provided care at no cost to qualified participants.

Sponsored by University of Georgia

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Expert Care in Athens

Access dyslipidemia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related dyslipidemia treatment provided free

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Check if you qualify for this dyslipidemia clinical trial in Athens, GA

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Why Participate?

  • No-Cost Study Care

  • Local to Athens

    Convenient for GA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Athens site if eligible
  4. 4Begin participation

About This Dyslipidemia Study in Athens

Cardiovascular disease risk factors, including higher BMIs and poor cholesterol profiles, are on the rise and contribute to the United States' growing disease burden. Cottonseed oil (CSO) is found readily in the food supply, and the investigator's previous studies have demonstrated that incorporating CSO into the diet is sufficient to improve fasting and postprandial blood lipids and other markers of chronic disease risk in both healthy and at-risk populations. This study aims to examine the impact of intermittent CSO consumption at different doses (consumed three times per week (3x/wk)) on changes in fasting and postprandial lipid metabolism/blood lipids and markers of chronic disease risk. The specific aims are: \*Examine the impact of intermittent CSO consumption (3x/week) at two different doses on fasting and postprandial lipids. \*Examine the impact of intermittent CSO consumption (3x/week) at two different doses on other markers of chronic disease risk. Participants will be asked to: \*Consume provided meal replacement shakes and snacks 3 times per week for 56 days. \*Attend three bi-weekly (every other week) short visits for fasting blood draws, body measurements, and collection of the next two weeks' study materials. \*Attend two longer (5.5h) testing visits, which include eating a standardized breakfast meal and having blood drawn periodically before and after breakfast. Researchers will compare CSO-30, CSO-20, and Control groups (receiving no oil) to see if intermittent CSO consumption imparts the same health benefits as previously shown with daily doses of CSO.

Sponsor: University of Georgia

Who Can Participate

Inclusion Criteria

25-75 year-old men and women at increased risk for cardiovascular disease. Increased risk for cardiovascular disease will be defined by either elevated cholesterol profiles -or- overweight/obesity.
Elevated cholesterol profiles will be defined as:
"Borderline High" and/or "at risk" in two of more of the following variables (total cholesterol: 180-239 mg/dL, LDL cholesterol 110-159 mg/dL, triglycerides 130-199 mg/dL) --or--
"High" in total cholesterol (240 mg/dL and higher), LDL (160 mg/dL or higher), or triglycerides (between 200-350 mg/dL).

Exclusion Criteria

Probable familial hypercholesterolemia, defined by: total cholesterol greater than 290 mg/dL or LDL levels greater than 190 mg/dL plus a family history of myocardial infarction (MI) before 50 years of age in a 2nd-degree relative or below age 60 in a 1st-degree relative.
Women on hormone replacement therapy less than 2 years.
Women who are pregnant or nursing/breastfeeding
individuals who regularly exercise more than 3h/w
weight gain or loss of more than 5% body weight in the past 3 months
plans to begin a weight loss/exercise regimen during the trial
history of medical or surgical events that could affect digestion or swallowing
gastrointestinal surgeries, conditions, or disorders
any chronic diseases (including moderate to severe asthma, chronic lung disease, and kidney disease),
metabolic disease
atherosclerosis
previous MI or stroke
fasting blood glucose levels greater than 126 mg/dL
blood pressure greater than 180/120 mmHg
medication use affecting digestion, absorption, or metabolism (e.g. thyroid meds), lipid-lowering medications, medications for diabetes, steroid/hormone therapies, or current antibiotic cycles
medically prescribed or special diets
Food allergies (specific to the foods in the study, including soy, dairy, gluten, Yellow No. 5, cottonseed oil, palm oil, and coconut oil)
fish oil supplements
excessive alcohol use (greater than 3 drinks/day for men; greater than 2 drinks/day for women)
tobacco or nicotine use
underweight BMI (\<18.5 kg/m²)

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Athens?

Yes, this clinical trial (NCT07246408) has an active research site in Athens, GA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Dyslipidemia Treatment Options in Athens, GA

If you're searching for dyslipidemia treatment options in Athens, GA, this clinical trial (NCT07246408) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Athens research site is actively enrolling participants for this clinical trial. You'll receive care from experienced dyslipidemia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all dyslipidemia clinical trials near you to find additional studies recruiting in your area.

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