RecruitingOBSERVATIONAL

French Cohort of Myocardial Infarction Evaluation

The FRENCHIE study is collecting information from people in France who have recently had a heart attack. Doctors want to understand patients' health, the medical care they receive, and their recovery over several years. Even though heart attack treatments have improved a lot, we don't fully know how these changes affect patients' health in the medium and long term. This study aims to fill that gap. By looking at a large group of patients, researchers hope to find out if certain treatments or ways of caring for patients lead to better health outcomes in the future. This information will help improve care for heart attack patients everywhere.

At a glance

Status

Recruiting

Sponsor

Assistance Publique - Hôpitaux de Paris

Enrolment target

30,000

Start

11 Mar 2019

Estimated completion

22 Mar 2049

Acute Myocardial Infarction

What is this study about?

Imagine you've just had a heart attack. Many doctors and nurses are working hard to help you. Over the last 20 years, we've gotten much better at treating heart attacks both when they happen and afterwards. But what we don't know enough about is how these new treatments and ways of looking after patients really affect people in the years following a heart attack.

This study, called FRENCHIE, aims to find out exactly that. It's like putting together a big puzzle. Researchers are collecting a lot of information from patients in intensive care units across France who have had a heart attack. They want to understand things like your age, other health conditions you might have, the exact type of heart attack you experienced, and all the treatments you received.

Then, they'll follow these patients over time, using information from national health records. This helps them see how different factors like your initial health, the care you got, and how you were followed up on, are linked to your health outcomes in the future. The main goal is to improve how we care for heart attack patients so that more people can live healthier lives for longer after experiencing a heart attack.

Key takeaways

The study helps doctors understand long-term heart attack recovery.
It uses existing medical information, so no extra tests for you.
Aims to improve future heart attack care for everyone.
Your care will not be affected if you join or don't join.
Your privacy is protected.

Who may be eligible?

You might be able to take part in this study if you've recently had a heart attack, specifically within 48 hours of your symptoms starting. Doctors will confirm your heart attack using blood tests (like troponin or CPKMB levels) and by looking at your symptoms, heart tracings (ECG), or new changes in your heart scans.

You also need to be 18 years old or older and covered by the French health insurance system. You'll need to give your written permission to join the study.

You wouldn't be able to join if your heart attack was caused by a medical procedure (like surgery), or if doctors later found out that your symptoms were actually due to something other than a heart attack.

Could this study suit you?

Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.

Have I had a heart attack very recently (within 48 hours of symptoms)?
Am I 18 years old or older?
Am I covered by French medical insurance?
Was my heart attack NOT caused by a recent medical procedure?
Could I give written permission to take part?

Answer every question to see your result.

What does participation involve?

If you take part, you won't be doing anything new or different than standard care. This is an 'observational study,' meaning doctors will simply collect information about your health and the care you're already receiving. You won't be given any experimental medicines or special treatments. Researchers will gather details about your heart attack, your usual hospital care, and how you're looked after after you leave the hospital.

They will also link your hospital records with national health databases in France to follow your health and any medical care you receive over time. This helps them see the long-term impact of your heart attack and treatment. The study uses existing information, so you won't have extra hospital visits or assessments beyond what your doctor already recommends for your care. The duration of follow-up can be quite long, as they are looking at mid- and long-term outcomes.

Potential risks and benefits

There are no direct risks to taking part in this study because you won't be undergoing any extra tests or treatments. Your medical information will be kept private. While you won't personally benefit directly from taking part, the information gathered will be extremely valuable. It will help doctors in the future understand how best to treat and care for heart attack patients, potentially leading to better health outcomes for many people. You are always free to change your mind and withdraw from the study at any time without it affecting your medical care.

Locations (1)

Hôpital Bichat, AP-HP
Verified postcode
Paris, France· Recruiting

Common questions

What is the main goal of this study?

The main goal is to understand how current heart attack treatments affect patients' health in the long run, years after their heart attack.

Will I receive any new treatments or medicines?

No, you will not receive any new or experimental treatments. The study just observes your standard care.

Who can join this study?

Adults (18+) in France who have recently had a heart attack and are covered by French health insurance may be eligible.

Will my personal information be kept secret?

Yes, all your medical information will be kept private and handled with strict confidentiality.

What do I need to do if I take part?

You don't need to do anything extra. Researchers will just gather information from your medical records and national databases about your health and care.

How to find out more

Tabassome SIMON

tabassome.simon@aphp.fr 01 40 01 13 93 Official trial record

Always speak to your GP or specialist before deciding to take part in a study.