Prospective Multicenter Registry of Gender, Diversity and Inclusion (GEDI) of Women With Acute Coronary Syndrome
Recruiting
Observational Study
Acute Coronary Syndrome
Gender
Genetic Predisposition
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 100
- Sex
- Female
- Study type
- Observational
- Participants needed
- 100 (estimated)
- Sponsor
- IRCCS San Raffaele · Other
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About This Trial
Create a multicenter prospective registry that collects information from women affected by acute coronary syndrome (ACS). This registry aims to understand the diversity in the presentation of women with ACS. It proposes to conduct a thorough characterization of the women involved in the study through genetic, biochemical, and molecular analysis.This approach aims to identify any differences in the…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Women \>/= 18 years with ACS (STEMI, NSTEMI or Unstable Angina).
Exclusion Criteria:
* age \< 18 years and/or unwillingness to sign informed consent and/or unwillingness to make follow-up visits
Contacts