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Completed

NCT Number: NCT02144922

Effect of Pitavastatin on Coronary Flow Reserve in Hypertensive Patients

Although statins reduce cardiac events in hypertensive patients with cardiovascular risk factors, the effect of statins on coronary flow reserve (CFR) has not been examined in such patients. The investigators hypothesize that pitavastatin added to standard antihypertensive therapy will be superior to placebo in improving CFR in hypertensive patients with cardiovascular risk, and try to examine this hypothesis in a double-blind, randomized comparison study using Doppler echocardiography.

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Key information

Age range

35 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Asan Medical Center

Seoul, 138-736, South Korea

About this study

Statin treatment improves coronary flow reserve (CFR) and decreases cardiac morbidity and mortality in patients with coronary artery disease (CAD) and hypercholesterolemia. Endothelial dysfunction and impairment in coronary microcirculation is also observed in hypertensive patients with cardiovascular risk factors. However, the measurement of CFR has rarely been performed in hypertensive patients without CAD, because CFR could be invasively measured using a Doppler guide wire in a cardiac catheterization laboratory. Recent advances in echocardiographic imaging techniques have made it possible to measure coronary flow velocity and CFR, which highly correlates with the CFR measured by invasive means.

Lipid lowering with a statin provided beneficial effects in patients with average levels of serum total cholesterol in the Anglo-Scandinavian Cardiac Outcomes Trial-Lipid Lowering Arm (ASCOT-LLA) study conducted in hypertensive patients at cardiovascular risk. Improvements in endothelial dysfunction and CFR may be related to the beneficial effects of statins in hypertensive patients without hypercholesterolemia, but the effect of statins on CFR has not been examined in such patients. Accordingly, the investigators try to examine the hypothesis that pitavastatin added to standard antihypertensive therapy in hypertensive patients with cardiovascular risk will be superior to placebo in improving CFR in a double-blind, randomized comparison study using Doppler echocardiography.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Controlled Hypertension: treated SBP<140 mmHg and DBP<90 mmHg
  • LDL cholesterol ≥ 130mg/dL
  • Patients with statin-naive state, defined as receiving no statin therapy for more than 6 months during the previous 12 months.
  • Any 1 of these cardiovascular risk factors required: smoking, age over 55 (men) or 65 (women), history of cerebrovascular event, family history of early CHD before age 55, HDL cholesterol < 40 mg/dL

Exclusion criteria

  • A previous history of intolerance or hypersensitivity to statins
  • Uncontrolled hypertension; SBP≥140 mmHg or DBP≥90 mmHg
  • Previous MI or currently treated angina pectoris
  • Stroke, TIA < 3 months
  • Secondary hypertension
  • Fasting serum triglyceride > 500 mg/dL
  • Clinical congestive heart failure
  • Uncontrolled arrhythmia
  • Left ventricular hypertrophy: LV mass index >134g/m2 (male) or >110g/m2 (female)
  • Concomitant clinically important hematological, gastrointestinal, hepatic, renal or other disease
  • Pregnant or lactating women and those of child-bearing potential
  • Diabetes
  • Peripheral vascular disease
  • Unwillingness or inability to comply with the procedures described in this protocol

Treatment and study plan

Pitavastatin

Drug

statin

Other names: Livalo

Control

Other

Life style modification alone

Primary outcomes

  1. change in the CFR value

    Time frame: 12 months

    Change of coronary flow velocity reserve from baseline to 1 year follow-up. For each patient, the averaged value of coronary flow velocity reserve will be obtained at baseline and 1 year follow-up.

  2. Difference in mean CFR value

    Time frame: 12 months

    DIfference in CFR value at 12 month follow-up between pitavastatin and placebo arm

Secondary outcomes

  1. change of CRP

    Time frame: 12 months

    Change of CRP from baseline to 1 year follow-up.

  2. Change of LDL-cholesterol

    Time frame: 12 months

    Change of LDL-cholesterol from baseline to 1 year follow-up.

  3. Change of averaged peak diastolic velocity

    Time frame: 12 months

    Change of averaged peak diastolic velocity from baseline to study end.

Sponsors and collaborators

Lead sponsor

Asan Medical Center

Other

Collaborators

  • JW Pharmaceutical

Registry information

Official study title

Effect of Pitavastatin on Coronary Flow Reserve in Hypertensive Patients With Cardiovascular Risk

Acronym: EPOCH

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
May 22, 2014
Registry last updated
Oct 14, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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