The SCCS Polypill Pilot Trial
| Status: | Completed |
|---|---|
| Conditions: | High Blood Pressure (Hypertension), High Cholesterol |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 45 - 75 |
| Updated: | 8/15/2018 |
| Start Date: | December 2015 |
| End Date: | June 27, 2018 |
In this study the investigators will examine the effect of the polypill on medication
adherence, systolic blood pressure, and LDL cholesterol over a 12 month span.
adherence, systolic blood pressure, and LDL cholesterol over a 12 month span.
The purpose of this study is to assess if a polypill-based approach to primary CVD prevention
is feasible in a low socioeconomic status population. The study will assess whether a
polypill approach is associated with better cardiovascular risk factor control compared with
usual care.
The polypill will be supplied as a compounded pill containing atorvastatin 10 mg, amlodipine
2.5 mg, losartan 25 mg, and hydrochlorothiazide 12.5 mg. The medications in the polypill have
been extensively evaluated individually and in combination. Each of the medications in the
polypill is approved by the United States Food and Drug Administration (FDA) and widely
administered in the US for the treatment of and prevention of cardiovascular disease. The
doses of each component medication included in the polypill are low, which should minimize
the chance of any potential side-effects.
In this study we assess medication adherence, systolic blood pressure, and LDL cholesterol
over a 12 month span, in subjects taking the polypill versus subjects under usual care.
is feasible in a low socioeconomic status population. The study will assess whether a
polypill approach is associated with better cardiovascular risk factor control compared with
usual care.
The polypill will be supplied as a compounded pill containing atorvastatin 10 mg, amlodipine
2.5 mg, losartan 25 mg, and hydrochlorothiazide 12.5 mg. The medications in the polypill have
been extensively evaluated individually and in combination. Each of the medications in the
polypill is approved by the United States Food and Drug Administration (FDA) and widely
administered in the US for the treatment of and prevention of cardiovascular disease. The
doses of each component medication included in the polypill are low, which should minimize
the chance of any potential side-effects.
In this study we assess medication adherence, systolic blood pressure, and LDL cholesterol
over a 12 month span, in subjects taking the polypill versus subjects under usual care.
Inclusion Criteria:
- Enrolled at the SCCS site in Mobile, Alabama, obtain care at Franklin Primary Health
Center, or live in the surrounding area.
- Aged 45-75 years
- Baseline systolic blood pressure ≥120 mm Hg. In this open-label trial, the study
physicians are permitted to prescribe any additional medication deemed appropriate to
achieve blood pressure control.
Exclusion Criteria:
- History of coronary heart disease or stroke
- History of cancer, except for basal cell skin cancer
- History of liver disease, not including chronic, clinically-stable hepatitis
- Laboratory evidence of hepatic dysfunction (an alanine aminotransferase level more
than two times the upper limit of the normal range)
- Known renal disease, estimated creatinine clearance < 60
- Current use of more than 2 anti-hypertensive medications
- LDL cholesterol ≥190 mg/dl
- Insulin-dependent diabetes
- Known intolerance to any of the components of the polypill
- Potassium <3.4 or >5.5 mEq/L
- Use of medications that interact with statins, including those affecting the
cytochrome P450 system
- Current use of diuretics for indications other than hypertension
- Comorbidities that might be expected to limit lifespan during the 12-month follow-up
period
- Inability to provide consent.
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