Do you have high cholesterol? We may have a medical research study for you

Updated on 23 November 2020


Do you have high cholesterol? We may have a medical research study for you


Coastal Carolina Research Center is seeking volunteers for an upcoming high cholesterol research study.

We will be evaluating the effectiveness of an investigational medication versus placebo in persons who have high cholesterol and who have LDL cholesterol ("bad cholesterol") levels between 130 and 220 determined by lab tests.

To be considered for participation in this research study, you must be between 18 and 80 years of age.Medical staff at our center will review additional criteria with you to determine if you are eligible.The study will consist of 9 visits over 12 weeks.

If you are eligible and decide to participate, volunteers will receive the following study-related care at no cost including:

  • Study medication or placebo
  • Physical exams
  • Lab work including cholesterol checks
  • ECG

Monetary compensation is available for those who qualify. No health insurance is required. Your information is maintained confidentially.

If you are interested or know anyone else who may be interested, please contact Coastal Carolina Research Center at 856-3784 (856-DRUG). You may also submit your interest by applying online at or by texting STUDY to 72727. Thank you for your interest and please contact us as soon as possible for this important cholesterol research study.

Condition High Cholesterol (Hyperlipidemia)
Clinical Study IdentifierTX138811
Last Modified on23 November 2020


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Inclusion Criteria

Furthermore, the study is seeking the following
Persons who are currently treating their cholesterol with a statin medication
Be in overall good health
If female, must be surgically sterile or post-menopausal
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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