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OpenTrials
Completed

NCT Number: NCT00987181

Non-Contact Measurement of Aortic Compliance

Reduced aortic stiffness is a powerful way to predict the outcome of cardiovascular (CV) disease. There are several non invasive methods for its estimation, most of which are based on the measurement of speed of the arterial pulse wave. (The stiffer the artery, the faster the pulse wave travels.) They rely on detecting the arterial pulse with 2 sensors placed on the skin a known distance apart and measuring the time for the pulse to travel between them. However all current methods require skilled operators and are of limited accuracy. Thus, there is a need for an easy to use and reliable device to measure pulse speed. The aim of this project is to develop a non contact device to detect the aortic pulse as it moves into the small arteries following the ribs, using the principle of thermal imaging, by means of a high sensitivity infra red camera, directed towards the subjects back. The investigators plan to validate the device and conduct a small feasibility study in patients undergoing elective angiography, by simultaneously measuring pulse speed using established methods. These are Doppler ultrasound (non-invasive) and direct intra-arterial measurement (the gold standard).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

London Chest Hospital

London, E2 9JX, United Kingdom

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 years and above
  • Patients eligible for coronary angiography
  • Informed consent obtained
  • Able to complete experimental protocol

Exclusion criteria

  • Refusal of consent
  • Age below 18 years
  • Breast feeding
  • Known or suspected pregnancy
  • Patient participating in another study at time of study entry or previous participation in this registry
  • diagnosed but untreated hypertension

Treatment and study plan

Primary outcomes

  1. Quantitative agreement between intra-arterial measurement of aortic pulse wave velocity and transcutaneous values: a) Contact PPG from probes on the skin of the back in the intercostal spaces and b) non-contact from infra-red camera imaging the back.

    Time frame: Single measurement to be made between January 2010 and June 2010

Secondary outcomes

  1. Assessment of differences in aPWV and between low and high risk groups of patients undergoing elective coronary angiography.

    Time frame: Single measurement to be made between January 2010 and June 2010

Sponsors and collaborators

Lead sponsor

Barts & The London NHS Trust

Other

Collaborators

  • National Institute for Health Research, United Kingdom

Registry information

Official study title

Non Contact Measurement of Aortic Pulse Wave Velocity

Important dates

Study start
2010
Primary completion
2012
Study completion
2013
First posted
Sep 30, 2009
Registry last updated
Feb 23, 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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