Status and phase
Conditions
Treatments
About
The objective of this study is to evaluate the effects of adding Tricor 145 mg to once daily atorvastatin 20 mg on CHD lipid laboratory parameters.
Enrollment
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Ages
Volunteers
Inclusion criteria
Subject is >= 18 years of age, any race, and any gender.
Subjects must have the following fasting parameters:
Subjects must have one or more of the following:
Subject has, in the opinion of the investigator, a life expectancy greater than 6 months.
Female subjects must have a negative pregnancy test prior to study enrollment.
Female subjects of child bearing potential must agree to practice an effective barrier method of birth control for the duration of the study.
Subject must be willing to observe the Step I Diet recommended by the NCEP throughout the study.
Subject must be willing to participate in the study and to complete all follow-up assessments.
Exclusion criteria
Primary purpose
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Interventional model
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Data sourced from clinicaltrials.gov
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