AMPM RESEARCH CLINIC
Frequently Asked Questions
Please review our list of frequently asked questions (FAQs) below to learn more about medical research. If you have questions that are not addressed in the FAQs, please contact one of the following persons.
To learn more about studies that are open for enrollment, please review the relevant research area on our website to see if any volunteers are needed. If you would like additional information on how to enroll for a study, contact: doctors@ampmrc.com
What is a clinical trial?
A Clinical Trial is a medical research that determines the safety and effectiveness of a drug or treatment and discovers any side effects. These trials do follow guidelines placed by US Food and Drug Administration (FDA) in order to ensure your safety.
What is the process of a clinical trial?
First, a screening interview where patient information will be taken concerning your medical history, medications, and other preliminary questions to make sure you fit the study requirements.
Second will be the informed consent process where you will receive materials that explain the study and how you will participate.
Third and final step is the medical assesment and medication. Once you are enrolled in a study, you may receive a study-related physical exam, study medication, laboratory tests, and study procedures as necessary, all free of charge. During the course of the study, medical personnel will meet with you to monitor your progress.
How do I learn about other studies?
You can register to be part of our volunteer database and we will get in touch with you if you may qualify for a study.
Why should I participate?
You may have access to advanced treatments before they are widely available and your participation will help others in need of these. Also, all studies are provided for free and may also include compensation for your time and travel.
Will I be compensated?
Yes, we understand your time is valuable and compensation is provided for time and travel. Please note that every study has different rates of compensation.
Are there any risks?
Your safety is always our main concern. All procedures are first reviewed by an independent Investigational Review Board (IRB) before they are administered. This assures that the study is ethical and the risks are as low as possible and worth any potential benefits. Also, these trials follow guidelines placed by US Food and Drug Administration (FDA) in order to ensure your safety. All details and risks of the study will be explained to you during the informed consent. You are welcome to take your time reviewing the consent form and ask any questions that you may have.