New cardiovascular clinical studies are now enrolling
Those who qualify may receive*:
- Payment of up to $440
- Study-related care from local doctors at no cost
- Study medication at no cost
- Compensation for time and travel
- Compensation for time and travel
There is no obligation, so see if you may qualify now.
Diagnosed with chronic heart failure?
ClinicalResearch.com is created by IQVIA, a trusted global provider of clinical research services. Our mission is to make it easier for people to learn about clinical trials and explore opportunities that may be a good fit.
Heart Disease Research
We're looking for individuals with a history of heart disease to potentially take part in studies designed to advance medical understanding and improve future care.
Our studies explore how safe investigational medications are for supporting overall cardiovascular wellness.
Why Participate?
Many people choose to participate in clinical trials to contribute to medical science and help advance new ways to support heart health and patient care.
Getting Started
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Answer a few questions to see if there's a current study that might match your profile
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No obligation to take part, and you don't need health insurance to be considered
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Your time and interest matter - help move medical research forward
MegaScreener
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A clinical trial, also called a clinical research study, is a carefully designed scientific evaluation of an investigational medicine or treatment. Clinical trials are conducted by doctors and researchers. Clinical research helps doctors and scientists determine if an investigational medicine or therapies are safe and/or effective for use in humans to potentially treat a condition, disease, or disorder.
Before regulatory authorities that are responsible for approving medicines for use in each country can consider an investigational medicine, device, or procedure for approval, it must be shown to be both safe and work well, or the overall benefits outweigh the risks. Typically, this is accomplished through clinical trials.
Clinical trials must be reviewed by an Institutional Review Board (IRB) or Ethics Committee (EC). An IRB or EC is a group that is responsible for helping to protect the rights and welfare of study participants. In addition, every study participant is monitored with medical tests and study-related exams before, during, and sometimes even after the trial.
If you are interested in participating, please fill out the online questionnaire below to see if you are eligible for the study. If you are potentially eligible, we will match you to a clinical research site in your area that is participating in the Auτonomy Study and seeking participants. Someone from the clinical research site will contact you to explain more about the study and to determine if you meet the study criteria before you make your decision about participating. The site team will provide you with more details about the study and determine your next steps.
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