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Clinical Trials/NCT07181317
NCT07181317RecruitingNot Applicable

WAMIF: Prospective Study in Young Women Presenting Acute Myocardial Infarction in France: Clinical, Morphological and Biological Descriptive Analysis: Cohort Follow up

French Cardiology Society1 site in 1 country314 target enrollmentStarted: November 25, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
314
Locations
1
Primary Endpoint
Death from any cause

Study Overview

Brief Summary

The WAMIF study was conducted from 2017 to 2019, including 314 patients in 30 French research centers spread across metropolitan France. It systematically collected the clinical, morphological, and biological characteristics of myocardial infarction cases affecting women under 50 years of age and assessed their short-term (in-hospital) and medium-term (12-month) prognosis. Extending the follow-up beyond 12 months for this first study would provide fundamental data for understanding and improving the care of these patients.

Detailed Description

The WAMIF study was conducted from 2017 to 2019, including 314 patients in 30 French research centers spread across metropolitan France. It systematically collected the clinical, morphological, and biological characteristics of myocardial infarction cases affecting women under 50 years of age and assessed their short-term (in-hospital) and medium-term (12-month) prognosis. The main results were: a particularly high incidence of modifiable risk factors affecting 86% of patients, with smoking being the primary cause in 75% of them.The clinical presentation found chest pain in more than 90% of cases. The pathophysiological forms of acute coronary syndrome identified the culprit artery in 90% of cases, a form without obstruction (MINOCA) was found in 17.8% of ST segment elevation infarctions (STEMI), spontaneous dissection in 14.6% of STEMI and 16.3% of NSTEMI.At 12 months, follow-up showed no cardiovascular deaths and two deaths related to neoplastic causes. At the end of this follow-up, 90% had no events. Compared to existing studies, these event rates are extremely low. Extending the follow-up beyond 12 months for this first study would provide fundamental data for understanding and improving the care of these patients. The secondary objective is the evaluation of the quality of life and mental health of women who have had an MI before the age of 50 years at a distance from the acute event.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All patients who participated in the WAMIF study (research registration number with the French Ministry of Health : 2015-A01263-46 / Protocol registration with Clinical Trials NCT03073447) and wish to continue follow-up in the study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Death from any cause

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who died from any cause since their participation in WAMIF study

Cardiovascular death

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who died from cardiovascular cause since their participation in WAMIF study

Stent thrombosis

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who had stent thrombosis since their participation in WAMIF study

Stroke

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who had stroke since their participation in WAMIF study

Recurrent myocardial infarct

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who had recurrent myocardial infarct since their participation in WAMIF study

Emergency revascularization

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who had emergency revascularization since their participation in WAMIF study

Major bleeding

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who had since major bleeding their participation in WAMIF study

Emergency hospitalization for heart failure

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who had emergency hospitalization for heart failure since their participation in WAMIF study

Emergency department visit

Time Frame: 5 to 10 years after the participation in WAMIF study

Number of patient who went to emergency department since their participation in WAMIF study

Secondary Outcomes

  • Anxiety score(5 to 10 years after the participation in WAMIF study)
  • Stress score(5 to 10 years after the participation in WAMIF study)
  • Depression score(5 to 10 years after the participation in WAMIF study)
  • Quality of life score(5 to 10 years after the participation in WAMIF study)

Investigators

Sponsor
French Cardiology Society
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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