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Clinical Trials in France / NCT07181317
Recruiting Observational

WAMIF: Prospective Study in Young Women Presenting Acute Myocardial Infarction: Cohort Follow up

NCT07181317 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2025-11-25
Last updated
2026-01-12

Condition(s) studied

Myocardial Infarction, Acute

Investigational drug(s) / intervention(s)

QuestionnairesMajor events

Questionnaires: Assessment of stress and anxiety and quality of life after myocardial infarct: * Stress score: Perceived Stress Scale-4 (PSS-4) * Anxiety score: Generalized Anxiety Disorder-7 (GAD-7) * Depression score: Patient Health Questionnaire-9 (PHQ-9) * Quality of life scores: European Quality of Life-5 Dimensions (EQ-5D) and 12-Item Short-Form General Health Survey (SF-12)

Major events: Collection of information related to major events occurring since inclusion in the WAMIF study

Study 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.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hôpital de la Pitié Salpétrière Paris France Recruiting

More French Cardiology Society trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07181317 on ClinicalTrials.gov ↗ ← All trials in France