Sex-based differences in early mortality after myocardial infarction. National Registry of Myocardial Infarction 2 Participants.
V Vaccarino, L Parsons, N R Every...
https://pubmed.ncbi.nlm.nih.gov/10413733/Actively Recruiting
Led by IRCCS San Raffaele · Updated on 2026-04-03
100
Participants Needed
4
Research Sites
52 weeks
Total Duration
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
Prospective Multicenter Registry of Gender, Diversity and Inclusion (GEDI) of Women With Acute Coronary Syndrome
A
Alaide Chieffo, MD
V
Vega Rusconi
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
IRCCS San Raffaele
Lead Sponsor
Federico II University
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
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
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Have more questions? Get in touch with our team for quick support
V Vaccarino, L Parsons, N R Every...
https://pubmed.ncbi.nlm.nih.gov/10413733/Jean-Philippe Collet, Holger Thiele, Emanuele Barbato...
https://pubmed.ncbi.nlm.nih.gov/32860058/Nathaniel R Smilowitz, Asha M Mahajan, Matthew T Roe...
https://pubmed.ncbi.nlm.nih.gov/29246884/Chirag Bavishi, Sripal Bangalore, Dipen Patel...
https://pubmed.ncbi.nlm.nih.gov/26163903/Giulia Renda, Giuseppe Patti, Irene Marthe Lang...
https://pubmed.ncbi.nlm.nih.gov/30777407/Kannikar Wechkunanukul, Hugh Grantham, Raechel Damarell...
https://pubmed.ncbi.nlm.nih.gov/27532797/Stefan Agewall, John F Beltrame, Harmony R Reynolds...
https://pubmed.ncbi.nlm.nih.gov/28158518/Robert A Byrne, Xavier Rossello, J J Coughlan...
https://pubmed.ncbi.nlm.nih.gov/37622654/Birgit Vogel, Monica Acevedo, Yolande Appelman...
https://pubmed.ncbi.nlm.nih.gov/34010613/Jacob A Udell, Gregg C Fonarow, Thomas M Maddox...
https://pubmed.ncbi.nlm.nih.gov/29521450/IRCCS San Raffaele
Lead Sponsor
Federico II University
Collaborating Sponsor