HDL Cholesterol Clinical Trial
Official title:
Effects of High Dose Simvastatin vs. Atorvastatin on Baseline Lipoprotein Profiles, Apo-A-1 and C Reactive Protein
Summary:
Background: There is a lot of interest in the function and role of HDL to prevent and
mitigate atherosclerosis in patients who are at or near LDLc targets. Statins have variable
effects on HDLc which are accentuated in patients with a low baseline HDLc. Higher doses of
statins are being used more commonly in practice based on newer outcomes studies which find
greater benefits of the higher doses compared to lower or standard doses. This study is
testing FDA approved dosages of two commonly used statin medications.
Design: The study is designed to examine the effects of 80mg simvastatin and 80mg
atorvastatin on HDLc concentrations. Serum will be saved for a hopeful collaborative effort
with investigators at the U. of Washington who are able to do more advanced testing of HDL
particle functionality. Based on the first 13 patients studied at Indiana University, the
effects of these statins on HDLc concentrations vary greatly. It is unknown what impact
these concentration changes have on the functionality of the particles however. A
meta-analysis of 4 prospective trials published in JAMA in 2006 found that increasing HDLc
with statins was independently associated with regression of atherosclerosis as measured by
intravascular ultrasound.
Patients: Patients with low HDLc will be the primary population recruited. Exclusion
criteria include interacting medications, pregnancy, baseline hepatic disease or other
illnesses which would put patients at increased risk of statin side effects.
The subject will be asked to come in for all study visits in a fasting state (only water for
past 12 hours). Both blood pressure and pulse will be checked at the screening visit as well
as all study visits. The baseline (screening) visit will include the consenting process and
completion of the first section of the Data Collection Sheet to further screen for
appropriate inclusion and exclusion criteria. Subjects who are on a statin will need to have
an 8-week wash out period prior to beginning the trial. The subject and their primary
provider must agree to the washout.
At the screening visit for subjects not taking a statin drug, 13 ml of blood will be drawn.
The blood will be processed by the OCTRI Core Laboratory staff. All of the lipid parameters
(complete lipid profile, apoB, apoA1, hs-CRP) will be tested at the OHSU lipid core lab.
Some of the blood collected will be sent to the OHSU core lab for testing of ALT as well as
for obtaining the long-term storage sample. Blood samples will be frozen and stored on the
14th floor of the CHH building in the laboratory of the Oregon State University School of
Pharmacy. Samples will be batched for processing (see sample processing below). The lipid
profile and ALT from the screening visit will be processed within approximately one week. If
necessary laboratory parameters meet inclusion and exclusion criteria, the subject will be
scheduled for the first study visit. Encapsulated placebo will be given to the subject to
take in between the screening and first study visit.
At the screening visit for subjects taking a statin drug, the study will be described and
consent to enroll will be obtained but no bloodwork will be performed. Subjects will be
given an encapsulated placebo to take for an 8 week washout period. At the second screening
visit, blood will be drawn to ascertain baseline laboratory values as described above for
subjects not on a statin drug. The subject will then be scheduled for their first study
visit 2 weeks later.
The other laboratory parameters (hs-CRP, apoA1 and apoB) and all future bloodwork which is
not necessary for the ongoing conduct of the trial may be batched and processed
periodically. The ALT from the second study visit (after first course of study medication)
will be processed prior to the third study visit to confirm that ALT remains less than 3
times ULR. If ALT is elevated (>105 IU/L) at the second study visit, the subject will be
discontinued from the study and the subjects primary physician notified. Additionally, if
the subject complains of myopathy which is felt to be consistent with possible drug-induced
myositis, a creatine phospho-kinase (CPK) test will be ordered. Consistent with the product
package insert (PI) for both atorvastatin and simvastatin, therapy will be stopped and the
subject discontinued from the study if CPK is greater than 10X the ULR.
At the first study visit, the subject will be randomized by the OHSU Research Pharmacy to
receive either 6 weeks of 80mg atorvastatin or 6 weeks of 80mg of simvastatin. The subject
will be scheduled for follow-up 6 weeks from the trial entry date and asked to bring the
investigational drug vial back at the next visit. The subjects will also be given a diary to
record their daily dose of medication taken. A urine pregnancy test will be done at the
first and third study visit in all women who are not post-menopausal as defined as at least
6 months without menstruation over the age of 50. Women who do not meet the post-menopausal
criteria, are sexually active and not on any form of birth control will be counseled to
begin and remain on birth control for the duration of the trial. Inability or unwillingness
to comply with chosen birth control measures will result in exclusion from the trial. Women
of child bearing potential not on birth control at the time of the screening visit who are
willing to begin birth control will be scheduled for their first study visit not sooner than
6 weeks after their screening visit to allow time for implementation of chosen birth
control. Subjects who are on hormone replacement therapy (HRT) will be allowed to enroll
provided that their regimen is stable and not expected to change during the study period.
Subjects will be informed that if their regimen does change during the study, they will need
to be removed from the study.
At the second visit, the appropriate section of the Data Collection Sheet will be completed,
a pill count of remaining drug doses will be done and 13 ml of blood will be drawn and
processed as previously outlined. The subject will then be scheduled for follow-up in 6
weeks and leave without any study medicine.
At the third visit, the appropriate section of the Data Collection Sheet will be completed
and 13 ml of blood will be drawn and processed as previously outlined. The subject will be
given a 6 week supply of the second medication (as previously determined by first
randomization scheme) and scheduled for follow-up in 6 weeks.
At the fourth and final visit, the appropriate section of the data collection sheet will be
completed and 13 ml of blood will be drawn and processed as previously outlined.
In between study visits, the study staff will contact subjects by phone to remind them of
their next appointment and ask about any adverse effects or other problems that the subject
may be experiencing. In the event that the phone number of record becomes inactive, a letter
will be sent to the address of record.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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