Impact of Assessment and Management of Comorbidities in Internal Medicine on Cardiovascular Risk

Recruiting now · Not applicable

Conditions studied: Adverse Cardiac Event, Major Adverse Cardiac Events

In brief

The aim of assessing and managing cardiovascular risk is to avoid, limit or delay cardiovascular morbidity and mortality. Planned internal medicine hospitalization is developed around the management of cardiovascular risk in patients at high cardiovascular risk, whether in primary prevention or secondary prevention. During planned hospitalization, patients benefit from comprehensive, personalized and adapted care for their comorbidities and their CVRF (cardiovascular risk factors). This study will make it possible to evaluate this overall course of multidisciplinary management of comorbidities of patients at high cardiovascular risk.

Key facts

Study ID

NCT06204549

Run by

University Hospital, Montpellier

People needed

70

Starts

2024-05-21

Expected to finish

2027-11-21

Last updated by the study team

2025-09-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• High-Risk Cardiovascular patients either receiving:
• Primary prevention because they have never had a cardiovascular event but have several cardiovascular risk factors such as high blood pressure particularly resistant, metabolic syndrome, diabetes , dyslipidemia, metabolic steatosis
• Or secondary prevention because they have already had a major cardiovascular event such as ischemic heart disease, heart failure
• Aged 18 and over
• Patient benefiting from comorbidities assessment during their planned hospitalization in the internal medicine department.

You may not qualify if…

• Patient refusal
• Subject not registered in social security system
• Pregnant or breastfeeding woman
• Patient unable to give their informed consent, protected adult, vulnerable people
• Subject deprived of liberty by judicial or administrative decision

Where it is running

• University Hospital — Montpellier, France (enrolling)

Full record on ClinicalTrials.gov

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