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Completed

NCT Number: NCT01278732

Central Blood Pressure Over 24 Hours (ABPM) and Left Ventricular Mass

The investigators aim to investigate whether central systolic blood pressure, as measured during regular 24 hour ambulatory blood pressure monitoring (ABPM), is a better predictor of left ventricular mass than peripheral systolic blood pressure during ABPM.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Cardiology Department, Klinikum Wels-Grieskirchen, Wels, Upper Austria, Austria

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About this study

It seems obvious that central blood pressures are pathophysiologically more relevant than peripheral blood pressures for the pathogenesis of cardiovascular disease: it is central systolic pressure (cSBP) against the heart ejects (afterload), and it is central pulse pressure (cPP) that distends the large elastic arteries. Indeed, cSBP and cPP have been associated more closely with left ventricular hypertrophy and carotid atherosclerosis as markers of hypertensive end-organ damage than brachial pressures in various populations. However, in these studies office blood pressure measurements have been used. As ABPM measurements per se show a closer association with hypertensive end-organ damage than office measurements, and as the investigators have recently developed and validated a novel algorithm (ARCSolver) to calculate central blood pressures from peripheral waveforms, the investigators speculate that cSBP measured during ABPM may be the best predictor of left ventricular mass.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

> 18 years of age,

  • no intake of antihypertensive medications
  • should have an indication for ABPM (suspected arterial hypertension)

Exclusion criteria

  • no written informed consent
  • left ventricular hypertrophy due to other reasons than hypertension (hypertrophic cardiomyopathy, infiltrative cardiomyopathy, valvular heart disease, congenital heart disease)
  • inability to provide adequate echocardiographic readings
  • segmental contraction abnormalities of the left ventricle
  • contraindications for ABPM (lymphedema both arms)
  • other rhythm than stable sinus rhythm
  • unstable clinical condition, including recent severe infections

Treatment and study plan

No intervention performed

Other

no intervention is performed

Primary outcomes

  1. Left ventricular mass (m-mode echocardiography)

    Time frame: measured within 4 weeks from ABPM

Secondary outcomes

  1. urine albumine / creatinine ratio

    Time frame: measured within 2 weeks from ABPM but before antihypertensive treatment is started

Sponsors and collaborators

Lead sponsor

Klinikum Wels-Grieskirchen

Other

Collaborators

  • Austrian Society of Hypertension
  • European Regional Development Fund
  • I.E.M. (Stolberg, Germany)

Registry information

Official study title

Central Blood Pressure Over 24 Hours (ABPM) and Left Ventricular Mas

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Jan 19, 2011
Registry last updated
Apr 3, 2015

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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