Left Ventricular Ejection Fraction Clinical Trial

Left Ventricular Ejection Fraction Clinical Trial in Boone Grove IN

Looking for a new potential treatment option for your LVEF? Consider a LVEF research study that could advance treatment options and support people like you in the future.

Indication (Disease)

about the study

Diagnosed with LVEF at least 3 months ago? You did not choose to live with LVEF but you can decide what comes next. Participants for a LVEF research study are needed in your area. You can make a difference in your community. Your participation can help advance the development of LVEF treatment options.

We cannot explore a potential new treatment for chronic HF without you.

The EASi-HF Trial is looking to find out if a potential new treatment combination is effective and safe for people with LVEF and LVEF of 40% or higher, who are already receiving the best possible standard-of-care treatment.

Participants will receive trial-related care from local doctors at no cost. If you or a family member were living with heart failure at least 3 months ago, you or they may be able to take part in a clinical study. Taking part could help advance heart failure research and help future patients.

See if you or a loved one are eligible for the EASi-HF Trial today. The EASi-HF Trial might be suitable for you if you:

  • are 18 years of age or older
  • were diagnosed with chronic HF at least 3 months ago and have a left ventricular ejection fraction (LVEF*) of at least 40%
  • are already receiving treatment for your HF

*LVEF is a crucial measurement used in assessing heart failure.

Eligible volunteers will receive trial-related assessments, care, and trial treatment at no cost.

Learn more now.

Compensation

Paid up to $2000

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Frequently Asked Questions

What is a clinical trial?

A clinical trial is a research study designed to help researchers learn more about health conditions, treatments, prevention methods, or medical products. Clinical trials follow structured protocols and are conducted under regulatory oversight.

Why do people participate in clinical trials?

People participate in clinical trials for many reasons, including contributing to medical research, learning more about their health, or helping advance future treatment options. Participation is always voluntary.

Is participating in a clinical trial safe?

Clinical trials are reviewed and monitored by regulatory authorities and ethics committees to help protect participant safety. Each study includes specific safety guidelines and an informed consent process.

Do I have to participate if I sign up on this website?

No. Submitting your information allows us to notify you about studies that may be relevant to you. You are never required to participate in any study.

What happens after I submit my information?

After you submit your information, you may be contacted if a clinical research study becomes available that matches your interests and basic eligibility. You can decide whether or not to learn more at that time.

Will I be contacted for every study?

No. We only reach out when a study may be relevant based on the information you provided and the study’s eligibility criteria.

Is there a cost to participate in a clinical trial?

Many clinical research studies cover study-related procedures, but details vary by study. All information is provided before any decision to participate is made.

Will I receive treatment if I join a study?

Clinical trials may involve investigational treatments, standard care, or observation only, depending on the study. Participation does not guarantee access to treatment.

Can I leave a clinical trial after joining?

Yes. Participation in a clinical trial is voluntary, and participants can choose to withdraw at any time.

Who runs clinical trials?

Clinical trials are conducted by research institutions, healthcare providers, pharmaceutical or medical device companies, and contract research organizations.

How do I know if a study is right for me?

Each study has specific eligibility criteria and participation requirements. You will receive detailed information before deciding whether to participate.

Why should I provide my contact information?

Providing your contact information allows us to notify you when clinical research opportunities become available that may be relevant to you. There is no obligation to participate.

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You’ll be the first to know when opportunities open up in your area.

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