The CArdiac Imaging RegistrY Study

  • STATUS
    Recruiting
  • End date
    Dec 1, 2030
  • participants needed
    5000
  • sponsor
    Johann Wolfgang Goethe University Hospital
Updated on 2 July 2021
cancer

Summary

In this prospective longitudinal observational investigator-led single centre cohort study we will include patients undergoing cardio-CT for clinical reasons, to evaluate the role of cardio-CT terms of its diagnostic and prognostic value, as well as risk-benefit ratio.

Particular aims include:

  1. To determine the prevalence of CAD for age, gender, ethnicity relative to established risk models
  2. To determine associations between CAD severity and plaque type and:
  3. with traditional risk factors (arterial hypertension, diabetes, hypercholesterolemia, smoking)
  4. blood markers of increased cardiovascular risk
  5. To determine predictive associations of between CAD with outcome (endpoint definitions in appendix)
  6. To determine the risk-benefit ratio (number of subsequent interventions, complications, radiation exposure, late onset of cancer diseases, etc).

Description

Particular aims include:

  1. To determine the prevalence of CAD for age, gender, ethnicity relative to established risk models
  2. To determine associations between CAD severity and plaque type and:
  3. with traditional risk factors (arterial hypertension, diabetes, hypercholesterolemia, smoking)
  4. blood markers of increased cardiovascular risk
  5. To determine predictive associations of between CAD with outcome (endpoint definitions in appendix)
  6. To determine the risk-benefit ratio (number of subsequent interventions, complications, radiation exposure, late onset of cancer diseases, etc).

Details
Condition Myocardial Ischemia, Cardiac Ischemia, Coronary heart disease, Coronary Artery Disease
Clinical Study IdentifierNCT04936867
SponsorJohann Wolfgang Goethe University Hospital
Last Modified on2 July 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Adults (=/>18 years of age)
Able to provide informed consent
Clinical indication for cardio-CT in line with the latest clinical guidelines

Exclusion Criteria

standard contraindications to CT (in line with local roles and guidelines - please see Appendix)
known allergy to iodinated contrast agent
suspected acute kidney injury
unstable hemodynamic status or arrhythmias
suspected acute coronary syndrome
manifest thyrotoxicosis
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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