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Disparities in Myocardial Infarction Remodeling According to Gender (REMOVE 2)

U

University Hospital, Angers

Status

Enrolling

Conditions

Ventricular Remodeling
Myocardial Infarction

Treatments

Diagnostic Test: cardiac imaging to assess left ventricular volumes and function

Study type

Interventional

Funder types

Other

Identifiers

NCT06343844
49RC23_0070

Details and patient eligibility

About

Following myocardial infarction, female individuals demonstrate a poorer prognosis, characterized by elevated rates of mortality and heart failure. A primary hypothesis suggests unfavorable cardiac remodeling in women. This remodeling, defined as alterations in cardiac size and shape post-infarction, necessitates repeated non-invasive imaging for study.

Enrollment

1,650 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age > 18 years
  • First myocardial infarction with ST-segment elevation during the hospital phase
  • Coronary angiography performed within 72 hours of the infarction
  • Inclusion in the RIMA registry
  • Patient affiliated or beneficiary of a social security scheme; Signature of informed consent

Exclusion criteria

  • Patients already enrolled in the study
  • Poor understanding of the French language
  • Pregnant, breastfeeding, or postpartum women
  • Individuals deprived of liberty by judicial or administrative decision; Individuals receiving psychiatric care under coercion
  • Individuals subject to a legal protection measure; Individuals incapable of giving consent

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,650 participants in 1 patient group

case control registry
Other group
Description:
left ventricular remodeling measurement with cardiac echography
Treatment:
Diagnostic Test: cardiac imaging to assess left ventricular volumes and function

Trial contacts and locations

1

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Central trial contact

VIVIANE CASSISA; LOIC BIERE, PHD

Data sourced from clinicaltrials.gov

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