MAIN-IMAGE Registry

All comers registry with patients with chronic coronary syndrome or acute coronary syndrome who underwent intracoronary imaging during cardiac catherization. The aim is to identify plaque characteristics on OCT or IVUS that are associated with adverse cardiac events including myocardial infarction and atherosclerotic progression.

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Key information

Conditions

Coronary Artery Disease Arterial Occlusive Diseases Arteriosclerosis Cardiovascular Diseases Coronary Disease Heart Diseases Myocardial Ischemia Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Frankfurt University Hospital, Frankfurt am Main, Hesse, Germany

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

patients undergoing pre-intervention optical coherence tomography imaging

Exclusion criteria

Treatment and study plan

Primary outcomes

Major adverse cardiovascular Events (MACE)

Time frame: after 2 years

Study contacts

Contact information is provided by the study sponsor or research team.

Lena Seegers, MD

CONTACT

[email protected]

+4963016666

Sponsors and collaborators

Lead sponsor

Goethe University

Other

Registry information

Official study title

Multifactorial Analysis of Coronary Artery Plaques Using INtracoronary IMAGing for Exploration of Atherosclerotic Determinants and Progression - the MAIN-IMAGE Registry

Acronym: MAIN-IMAGE

Important dates

Study start: 2023
Primary completion: 2028
Study completion: 2031
First posted: Mar 12, 2024
Registry last updated: Mar 12, 2024

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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