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Taking people in ItalyNo phase

Registry studying women with acute coronary syndrome to understand differences in heart attack presentation

Collects information and samples from women with acute coronary syndrome to study how it presents.

Plain-language title generated from the registry record
Registry title: Prospective Multicenter Registry of Gender, Diversity and Inclusion (GEDI) of Women With Acute Coronary Syndrome

Key facts

Where
Milan and Naples, ItalySee the 4 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 100 years old?

Source: NCT06441942, who can take part

Where in Italy

  • Centro Cardiologico MonzinoMilan, ItalyTaking people
  • Fondazione IRCCS Cà Granda Ospedale Maggiore PoliclinicoMilan, ItalyTaking people
  • IRCCS San Raffaele HospitalMilan, ItalyTaking people
  • Azienda Ospedaliera Universitaria Federico IINaples, ItalyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
IRCCS San Raffaele
Trial code
NCT06441942
Record updated
3 April 2026
Original description
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 characteristics of women with ACS and to identify disease subtypes that may influence treatment options and clinical outcomes.Read full original descriptionShow less

Creation of a Prospective Multicenter Registry of Gender, Diversity and Inclusion (GEDI) in Phenotypic and Genetic Characterization of Acute Coronary Syndrome.

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 characteristics of women with ACS and to identify disease subtypes that may influence treatment options and clinical outcomes.

Inclusion: Women >/= 18 years with ACS (STEMI, NSTEMI or Unstable Angina).

Exclusion: age < 18 years and/or unwillingness to sign informed consent and/or unwillingness to make follow-up visits.

ClinicalTrials.gov NCT06441942