Left Ventricular Ejection Fraction Clinical Trial

• La Porte IN
• Actively Enrolling

Join the Study

Left Ventricular Ejection Fraction Clinical Trial in La Porte IN

Do not let fatigue associated with your LVEF hold you back. Learn about a new research.

Indication (Disease)

Left Ventricular Ejection Fraction

about the study

If you are 18 or older and were living with LVEF at least 3 months ago, you may be eligible to help us explore a potential new treatment option. You will continue to receive your existing LVEF treatment. Adults living with chronic heart failure need new treatment options. Join a clinical trial for people who are already receiving the best possible standard-of-care treatment. See if a heart failure clinical trial to help our research efforts is right for you.


The EASi-HF Trial is looking for individuals who are 18 years of age or older, were living with chronic HF at least 3 months ago and have a LVEF of at least 40%, and are already receiving treatment for their HF.
By joining the EASi-HF Trial, you may receive:

• trial-required investigational treatment
• trial-related care from local doctors at no cost
• reimbursement for trial-related travel expenses

Health insurance is not required to take part.


If you are interested in potential new treatment options for LVEF, see if aresearch is right for you. Participants will continue to receive their existingLVEF, treatment.

Enrollment is limited so act quicky.

Compensation

Paid up to $2000

Enrolling Patients Near

La Porte IN

Join the Study

See if you're eligible to participate.

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Join the Study

See if you're eligible to participate.

Click Here

• Last updated 5 months ago
• All Left Ventricular Ejection Fraction Research Site Locations
• Other Studies in La Porte IN

• Actively Enrolling

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.