Prospective Multicenter Registry of Gender, Diversity and Inclusion (GEDI) of Women With Acute Coronary Syndrome
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-100
SponsorIRCCS San Raffaele
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 characteristics of women with ACS and to identify disease subtypes that may influence treatment options and clinical outcomes.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Women >/= 18 years with ACS (STEMI, NSTEMI or Unstable Angina).
Disqualifiers
age < 18 years and/or unwillingness to sign informed consent and/or unwillingness to make follow-up visits
Trial population
The study will include female patients presenting with ACS (according to ESC guidelines)
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
100 Participants
are grouped into 1 trial groupGroup A: Case
Trial outcomes
Primary outcomes
1
Multicentric Registry
The aim will be to create a prospective multicenter registry of gender, diversity and inclusion (GEDI) of women with Acute Coronary Syndrome
Time frame
12 months of follow-upSponsors and contacts
Click on the lead sponsor to view all of their trials.
IRCCS San Raffaele
Lead sponsor
Federico II University
Collaborator
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Collaborator
Centro Cardiologico Monzino
Collaborator
Source ClinicalTrials.gov