Longitudinal Study of Multi-Analyte Profile for Dyslipidemia

Status unconfirmed · Not applicable

Conditions studied: Dyslipidemia

In brief

The primary objective of this study is to determine any changes in cardiovascular risk among individuals receiving a statin by assessing their multi-analyte profile.

Key facts

Study ID

NCT01441908

Run by

MaiHealth Inc

People needed

40

Starts

2011-06-01

Expected to finish

2012-04-01

Last updated by the study team

2012-04-16

Who can join

Age: 30 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Sign and Date IRB approved consent form
• Be between 30-65 years of age as of date of consent
• Have a total cholesterol value of 200-300 (units)
• Have an LDL cholesterol value of > 100 (units)
• Able to speak and understand English
• Willing and able to participate for the 6 months required by the study
• Willing and able to provide fasting blood specimens
• Women of child-bearing potential must have a negative pregnancy test at screening
• Medically (appropriate) eligible to take the statin as determined by PI

You may not qualify if…

• Have a body Mass Index (BMI) > or = 35
• Pregnant (or planning to become pregnant during the course of the study)
• Currently taking a statin or discontinued taking a statin within 9 months of the date of screening

Where it is running

• Wake Research Associates — Raleigh, North Carolina, United States

Full record on ClinicalTrials.gov

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