Cardiovascular disease in women.
Alan M Weiss
https://pubmed.ncbi.nlm.nih.gov/19231603Actively Recruiting
Age: 18Years - 100Years
FEMALE
ID06441942
Creation of a Prospective Multicenter Registry of Gender, Diversity and Inclusion (GEDI) in Phenotypic and Genetic Characterization of Acute Coronary Syndrome
Led by IRCCS San Raffaele · Updated on 2026-04-03
100
Participants Needed
4
Research Sites
52 weeks
Total Duration
On this page
Sponsors
I
IRCCS San Raffaele
Lead Sponsor
F
Federico II University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are creating a multicenter prospective registry to collect detailed information from women affected by acute coronary syndrome (ACS) across various Italian regions. This study aims to understand the diversity in how ACS presents among women from different cultural and ethnic backgrounds. The research will focus on identifying distinct disease subtypes that may affect treatment options and clinical outcomes by conducting genetic, biochemical, and molecular analyses. Women who join the study will be thoroughly characterized through clinical assessments, imaging, and molecular testing. The study will stratify participants by age and the type of coronary artery disease, distinguishing between obstructive and non-obstructive forms. Additionally, the research will evaluate socioeconomic status, health literacy, and awareness of risk factors among the participants. Participants will be followed for 12 months as part of the registry. During this time, researchers will collect and analyze data to better understand ACS in women. The study involves no specific treatment interventions but focuses on observation and data gathering to inform future care strategies. Women aged 18 to 100 with ACS will be enrolled, and follow-up visits will monitor their health status and disease progression.
CONDITIONS
Brief Title
Prospective Multicenter Registry of Gender, Diversity and Inclusion (GEDI) of Women With Acute Coronary Syndrome
Who Can Participate
Age: 18Years - 100Years
FEMALE
Eligibility Criteria
You may qualify if you...
- Women aged 18 years or older with acute coronary syndrome (STEMI, NSTEMI, or Unstable Angina)
You will not qualify if you...
- Age under 18 years
- Unwillingness to sign informed consent
- Unwillingness to attend follow-up visits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
1
2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Monitoring
Duration - 12 months
Participants with acute coronary syndrome are observed and characterized through clinical, imaging, genetic, biochemical, and molecular assessments.
Visits scheduled according to clinical and registry requirements
Trial Site Locations
Total: 4 locations
1
IRCCS San Raffaele Hospital
Milan, Italy Milan, Italy, 20132
Actively Recruiting
2
Centro Cardiologico Monzino
Milan, Milano, Italy, 20138
Actively Recruiting
3
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Milan, Milan, Italy, 20122
Actively Recruiting
4
Azienda Ospedaliera Universitaria Federico II
Naples, Napoli, Italy, 80131
Actively Recruiting
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Research Team
A
Alaide Chieffo, MD
V
Vega Rusconi
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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