Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06601270

SCAD : a Registry of Spontaneous Coronary Artery Dissection

A Registry of Spontaneous Coronary Artery Dissection

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,500 (estimated)
Sponsor
European Society of Cardiology · Network
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Spontaneous coronary artery dissection (SCAD) is an increasingly recognised cause of non-atherosclerotic acute coronary syndromes (ACS), predominantly afflicting young women without conventional atherosclerotic risk factors. Knowledge of SCAD has advanced considerably in the last few years as a result of data from a number of local and national registries 1-6. Like all rarer diseases however, a better understanding of SCAD will require international collaboration. At present, there is no European or International SCAD registry despite increasing recognition that there are key differences in the diagnosis, interventional and medical management of SCAD compared with conventional atherosclerotic ACS. The ESC-ACCA Study Group on Spontaneous Coronary Artery Dissection supported by the European Observational Research Programme will now build the first pan-European SCAD registry to advance our understanding of current management of this condition, inform guidelines, educate clinical colleagues and advance research.

Detailed description

Observational, multicentre, international retrospective and prospective cohort study. Since this is an observational study, a formal sample size is not necessary. At least 500 prospectively recruited patients and 500 historical cases will be enrolled. Patient data will be collected at the following time-points: * First SCAD event visit (retrospectively on chart review) * First follow-up: at time of enrolment * Yearly follow-up: up to 1, 2, 3, 4 and 5 years post enrolment or until study completion Approximately 30 countries and 120 sites will participate in this registry.

Conditions

Interventions

TypeNameDescription
OTHERThere are no interventions as the study is purely observational.There are no interventions as the study is purely observational.

Timeline

Start date
2021-01-30
Primary completion
2026-10-01
Completion
2027-10-01
First posted
2024-09-19
Last updated
2024-10-29

Locations

73 sites across 24 countries: Argentina, Austria, Belgium, Bosnia and Herzegovina, Brazil, Croatia, Cyprus, Czechia, Denmark, France, Germany, Greece, Iran, Italy, Netherlands, New Zealand, Norway, Poland, Portugal, Serbia, Singapore, Slovakia, Spain, United Kingdom

Source: ClinicalTrials.gov record NCT06601270. Inclusion in this directory is not an endorsement.