Actively Recruiting
The Positive Prognostic Value of Stress Echocardiography - AMPHIPOLIS STUDY
Led by Hellenic Society of Cardiology · Updated on 2025-02-21
390
Participants Needed
1
Research Sites
169 weeks
Total Duration
On this page
Sponsors
H
Hellenic Society of Cardiology
Lead Sponsor
U
University of Cyprus
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is a prospective, multicenter, observational study of patients with recent stress echocardiography positive for myocardial ischemia. Up to now 25 echocardiography labs form Greece and Cyprus have declared their intention to participate. The investigators will enroll 390 patients with a positive stress echo, who will undergo invasive coronary angiogram and then will be followed up for at least 6 months. The objectives are the following: 1. To assess the prognostic value of positive stress echo by monitoring for cardiovascular death and major adverse cardiovascular events (MACE) during the follow-up. 2. To investigate the relationship of stress echo findings with invasive coronary angiography anatomical findings. 3. The association of cardiovascular risk profile of participants with stress echo and coronary angiography findings.
CONDITIONS
Official Title
The Positive Prognostic Value of Stress Echocardiography - AMPHIPOLIS STUDY
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with recent stress echocardiography positive for any extent of myocardial ischemia
You will not qualify if you...
- Heart failure with reduced ejection fraction requiring viability study
- Any symptomatic valvular disease causing symptoms
- Established or suspected cardiomyopathy
- Chronic diseases reducing life expectancy such as active cancer, severe liver impairment, or autoimmune diseases
- Recent acute coronary syndrome within the last week
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hellenic Society of Cardiology
Athens, Attica, Greece
Actively Recruiting
Research Team
N
Nikolaos Kadoglou
CONTACT
I
Ioanna Metaxa
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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