Are you right for our studies?
Do You Want to Participate in Our Dermatology or Neurology Clinical Trials?
Did you know that clinical research studies are a great way to receive medical services at no cost while you learn more about your medical condition? At ACRI, we are seeking volunteers for our dermatological and neurological research studies and aim to make your experience with us a positive one.
From our friendly and knowledgeable staff to our commitment to respecting your time and investment. We also compensate our participants while providing diagnostic testing and careful evaluations from our board-certified medical doctors free of charge to the patient.
Are you right for our studies?
The Focus of Our Trials
Innovation requires diversity. That’s why we are on the lookout for a wide variety of individuals to participate in our trials. Through our clinical trials, we perform Phase II to IV safety and efficacy trials for dermatology and neurology pharmaceuticals. Your participation allows us to move forward on innovative solutions for a variety of dermatological and neurological treatments and research.
Questions About Joining Our Clinical Trials
Clinical trials are research studies that involve human volunteers to research medicines and treatment options for specific illnesses. They are the catalyst for developing and discovering successful treatment options. Before you decide to join our clinical trials, the medical doctor involved must discuss your rights and your role in the study. At ACRI, we thoroughly discuss the process before you join.
Before you can participate in the trial, your general medical history is taken and you must sign an Informed Consent Form (ICF) which goes into detail about the purpose of the study you’re involved in. This same form also covers the potential risks, benefits, and any financial compensation for the trial. We highly recommend talking to our doctors about any questions you may have before the trial begins. Keep in mind, you can withdraw at any time.
Clinical trials such as those at ACRI are governed by the same ethical and legal codes required for medical practice. In addition to this, clinical research trials are federally regulated and are structured with multiple safeguards to reduce risks for participants. Our team has detailed protocols to follow and are required to meet specific standards to ensure your safety. While these measures are taken to reduce risks for clinical trial participants, some reasonable risk is unavoidable due to the nature of medical research. You will be informed of all known risks associated with your trial through the Informed Consent document you are given before the trial.
As a participant in our trial, you can begin to take greater control over your health care. You also have an opportunity to access new research treatments before they are available to the public. This in turn enhances scientific study and research and contributes to the health of many individuals.