Welcome to Clinical Trials Info
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Additional Information on Clinical Trials
CLINICAL TRIAL FAQS
Why Should I Volunteer?
You may be wondering if you should volunteer for a clinical research study. You may have questions as to who sponsors these clinical trials, who is protecting your rights? Clinical trials are research studies that deliver new life-changing drugs — but they can’t happen without clinical trial participants. Participants in clinical trials can play a more active role in their own health care, gain access to new research treatments before they are widely available, and help others by contributing to medical research.
What are the benefits?
Clinical research studies can lead to the advancement of medical therapies to treat and help individuals around the globe with all different health conditions. You can assist in leading the medical industry as a participant in clinical research and also receive top medical advice and care at potentially no cost to you.
Who Sponsors the Study?
Clinical research studies are sponsored by government agencies and private organizations in an attempt to find better ways to treat diseases. Pharmaceutical companies working with medical centers, doctors’ offices, and the government sponsor studies to test their products.
Who Conducts the Study?
A research team made up of many different employees run the actual clinical studies. The head of the research team is the Principle Investigator. The Sub-Investigators are doctors and physician assistants. And finally, there are multiple coordinators who handle most of the administrative responsibilities of the clinical trial, act as a liaison between the office and the sponsor, and review all of the data records. Each person plays a critical role in completing the studies.
What Qualifications are Required for Studies?
Each study has different requirements that pertain to the volunteers. Age groups can differ and certain diseases or histories of diseases are not allowed while other specific diseases are sometimes required. If you are interested in volunteering for a study, our research team will gather information from you on your medical history in order to find out if you qualify for the study. You will also be told of the possible risks and benefits that come with being involved in the study through the informed consent process.
What is Informed Consent?
The informed consent is a process that takes place before you can join the study. During this process, you will be told what you can expect from the study. You will be told who will seek your personal medical information, and how it will be kept confidential. A consent form will also be given to you to read. You are encouraged to ask questions both about the study and parts of the consent form that are unclear to you. If you decide that you would like to be part of the study, you will be asked to sign the consent form. However, even after signing the consent form, you are allowed to change your mind and withdraw from the study at any time.
What are Study Controls?
An ethics committee must review each study before it is allowed to begin. It is known as the Institutional Review Board, or IRB. The committee is comprised of doctors, nurses, and people from the community who review the studies in order to protect the participants’ rights and safety. In addition, the Food and Drug Administration sets specific requirements for drug testing that are followed in every study.
For further information on clinical trials, please visit https://www.ciscrp.org
To find actively enrolling clinical trials, please visit ClinicalTrials.gov