Frequently Asked Questions
The purpose of clinical research is to determine how new medications and treatments work on people. By conducting clinical trials or studies, doctors help discover new and different ways to detect, diagnose, control, treat, and even prevent illnesses. Before a new medication or treatment is approved for use by the public, it is necessary to test it in great detail according to the strict rules and regulations of the U.S. Food and Drug Administration (FDA).
During a clinical study you will work with a research team in a doctor’s office. Members of the team include doctors, nurses, research coordinators, and other health care professionals. You will first be called in for an office visit to see if you qualify for the study. If you qualify, all the medical visits you make relating to the study will be at NO COST to you. These visits may include: physical exams, doctor visits, study medications, laboratory tests, etc. The amount of visits required will vary depending on the specific trial.
Volunteering to be involved in a clinical trial comes with many benefits:
- Free healthcare by qualified medical personnel, including doctor visits and study medication
- Having access to new medications and treatments before being available to the public
- Contributing to the advancement of new medications and technology in the healthcare industry
- Providing beneficial research to improve the quality of life for your children, grandchildren, and future generations
Patient safety and well-being is the number one priority of DM Clinical Research. Before participating in any aspect of the clinical study, a healthcare professional will review with you the Informed Consent. If you agree to participate in the trial, you must agree to and sign this form. The Informed Consent list details of the study, including possible risks. Throughout the study, you will be under the care of an experienced physician who has been trained and designated as the Principal Investigator of the study.
Furthermore, before studies are made available to the public they must be approved by an Institutional Review Board (IRB) IRB approval is required by the FDA to make sure that the right and well-being of patients are protected. Agreeing to participate in a clinical study is completely voluntary and you are free to leave it anytime if you so desire. DM wants you to feel assured and comfortable at all times.
There are several questions you may wish to consider before enrolling in a clinical trial:
- What is the purpose of this trial
- How long will the trial last
- Which treatments and tests will be used in the trial and how
- Who will pay for the treatment involved in this trial
- Will I be reimbursed financially for participating
- Who will be incharge of my care during the trial
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