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Effect of Intensive Blood Pressure Control on Progression of Coronary Atherosclerosis: Randomized Evaluation by Intravascular Ultrasound

Effect of Intensive Blood Pressure Control on Progression of Coronary Atherosclerosis: Randomized Evaluation by Intravascular Ultrasound

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01230216
Acronym
PREVUS
Enrollment
8
Registered
2010-10-29
Start date
2010-12-31
Completion date
2015-04-30
Last updated
2016-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Hypertension

Keywords

coronary artery disease, hypertension

Brief summary

The purpose of this study is to evaluate the effect of intensive blood pressure control compared to standard blood pressure control on progression of coronary atherosclerosis by intravascular ultrasound in hypertensive patients with coronary artery disease.

Detailed description

Antihypertensive therapy is reported to reduce cardiovascular events in patients with coronary artery disease. The goal of blood pressure in patients with coronary artery disease is recommended to control below 140/90mmHg. However, the effect of intensive blood pressure control compared to standard blood pressure control is still unknown. The purpose of this study is to evaluate the effect of intensive blood pressure control compared to standard blood pressure control on progression of coronary atherosclerosis by intravascular ultrasound in hypertensive patients with coronary atherosclerosis after 18 months. The goal of systolic blood pressure is under 120mmHg in intensive blood pressure control group and under 140mmHg in standard blood pressure control group. The design of this study is randomized control study.

Interventions

DRUGcontrol systolic blood pressure less than 120 mmHg

use losartan to control blood pressure

DRUGcontrol systolic blood pressure less than 140 mmHg

use losartan to control blood pressure

Sponsors

Takeshi Morimoto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 79 Years
Healthy volunteers
No

Inclusion criteria

* coronary artery diseases which require coronary angiography or percutaneous coronary intervention * primary hypertension (systolic blood pressure 140-180mmHg within one month)

Exclusion criteria

* severe hypertension * secondary hypertension * treated with more than three antihypertensive drugs * left main trunk trunk coronary artery disease * moderate heart failure * severe valvular disease * liver dysfunction renal dysfunction (Cr\>=2.0mg/dl) Pregnant or nursing women severe arrhythmia

Design outcomes

Primary

MeasureTime frameDescription
change of percent atheroma volume1.5-yearchange of percent atheroma volume measured by intravascular ultrasound

Secondary

MeasureTime frameDescription
all cause death1.5-yearDeath from any cause
cardiac death1.5-yearDeath from cardiac diseases
cardiovascular death1.5-yearDeath from cardiovascular diseases
myocardial infarction1.5-yearmyocardial infarction defined by ARC
stroke1.5-yearboth ischemic and hemorrhagic strokes excluding transient ischemic attack
target-lesion revascularization1.5-yeartarget-lesion revascularization
any coronary revascularization1.5-yearany coronary revascularization
hospitalization due to angina pectoris1.5-yearhospitalization due to angina pectoris
hospitalization due to heart failure1.5-yearhospitalization due to heart failure
change of total atheroma volume1.5-yearchange of total atheroma volume measured by intravascular ultrasond
percent change of total atheroma volume1.5-yearpercent change of total atheroma volume measured by intravascular ultrasound
change of atheroma volume at most severe 10mm lesion1.5-yearchange of atheroma volume at most severe 10mm lesion measured by intravascular ultrasound

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026