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OpenTrials
Completed

NCT Number: NCT01705054

Angina Prevalence and Provider Evaluation of Angina Relief

The purpose of this study is describe the frequency of chest pain and how chest pain impacts patients' quality of life in the outpatients with chronic coronary artery disease in contemporary cardiology practice settings.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Saint Luke's Hospital of Kansas City

Kansas City, Missouri, 64111, United States

About this study

The primary goals in the management of stable coronary artery disease (CAD) are to reduce risk factors for heart attack and to control the symptoms of angina (chest pain). Ideally angina is well controlled with medications alone, but invasive procedures are a valuable option for patients with persistent angina. The amount of angina among patients with stable CAD in the outpatient setting, however, is unknown. An Australian study reported that almost 1 in 3 patients with stable angina being treated by primary care doctors had angina at least once a week, which was associated with worse quality of life. We propose to examine the burden of angina in outpatients with stable CAD who are being medically managed by cardiologists in the United States through administration of a one-time survey. The information from this study could ultimately help improve management of stable CAD and angina and illuminate potential underuse of revascularization. While cardiologists are generally expected to provide better angina control than primary care doctors, establishing the prevalence of angina among the best providers will help with a framework for interpreting symptom control among other practitioners.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Coronary artery disease patients being seen in a participating cardiology office for a scheduled clinic visit who agree to take the survey.

Exclusion criteria

  • Too ill to take survey
  • Previously completed this survey
  • Refused to participate

Treatment and study plan

Primary outcomes

  1. Seattle Angina Questionnaire

    Time frame: One time cardiology office visit.

    Percentage of patients with frequent angina (>1 episode/week) as measured by the Seattle Angina Questionnaire (SAQ).

Secondary outcomes

  1. Quality of Life

    Time frame: One time cardiology office visit.

    Evaluate the impact of frequent angina on Quality of Life (as measured by the SAQ)

  2. Physician Perspective

    Time frame: One time cardiology office visit.

    Identifying differences between patients' and cardiologists' assessment of angina control

  3. Cardiology practices angina control.

    Time frame: One time cardiology office visit.

    Evaluate the differences in angina control between cardiology practices.

Sponsors and collaborators

Lead sponsor

Saint Luke's Health System

Other

Collaborators

  • Gilead Sciences

Registry information

Acronym: APPEAR

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Oct 12, 2012
Registry last updated
Oct 19, 2021

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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