For over 10 years The Arlington Research Center (ARC) has been serving our patients with cutting edge new treatments for various dermatological and infectious diseases. New trends in medicine and treatments have been the result of our efforts in safe medication testing with our patients.
We have a variety of research programs available to patients who are interested in participating in studies for new medical treatments, vaccines or studies of current medications.
For the majority of our studies participating patients will receive free medication, free office visits and treatment, as well as a small reimbursement for time and travel.
Our team of physicians, nurses and study coordinators will provide individualized attention to these study patients.
Much is advancing in the field of dermatology treatment. Dr. Moore and her team are actively participating and advancing discovery of new and innovative methods of treating a variety of skin issues. If you participate in a clinical trial, you too are contributing to the discovery and advancement of new medical treatments for skin and total body health. As a participant in a clinical trial you qualify to receive free medication and treatment. You may receive a small stipend as well for your time and travel. You may even potentially improve your specific skin condition and overall health.
Arlington Research Center only participates in trials that are safe for the majority of patients participating. We avoid studies that have high risks for participating patients. Many of the medications used in our trials are already on the market or soon to be on the market. You will be carefully screened to see if you qualify and are a safe candidate for the trial you are considering. You will also be informed in detail about any possible side effects of the medication you will be using. You will also be closely monitored while participating in the clinical trial. If there are any adverse reactions, you will be quickly treated and potentially removed from the trial if there are any concerns about your health and welfare. All clinical trials will adhere to a strict predetermined protocol that outlines exactly what will and may take place during the course of the study.
All information, including medical, personal, or other information obtained during a clinical trial, will remain confidential and is protected by state and federal regulations governing clinical research. Personal information will only be released with your explicit authorization. You will be informed as to what data will be collected by the clinical trial. Personal information such as name, address, phone number, etc. are never given to the pharmaceutical company gathering the clinical trial data.
In some studies all medical care related to the clinical trial, including exams, laboratory tests, and medications, is provided at no charge to you. Certain clinical trials may also reimburse you a flat fee to cover your travel and time expenses.
Each clinical trial is different. This information will be provided to you in the consent paperwork. Some studies last 4 to 6 weeks. Other studies may involve participation for 6 to 12 months. Most trials involve an office visit once every few weeks. The initial visit usually lasts 30-90 minutes, while subsequent visits may be far shorter.Some studies may ask you to call in occasionally or may ask you to keep a log of your condition over a number of days. All expectations about the use of your time will be clearly outlined in your clinical trial paperwork.
A board-certified physician will diagnose you and/or offer medical advice. Both the physician and a clinical research coordinator will determine if you are eligible for a specific clinical trial.
The clinical research team will determine whether you are an appropriate candidate for a clinical trial based on specific inclusion and exclusion criteria. These criteria will be described in detail in the consent paperwork and study protocol and may vary significantly between different clinical trials.
Inclusion criteria are characteristics that someone must have to join a clinical trial.Exclusion criteria are characteristics that someone cannot have in order to participate in a clinical trial.
You must be able to physically attend clinical visits in our office in Arlington, Texas. You must be able to keep all the appointments required for participation in the entire clinical trial. If you have plans to travel or will not be available for visits during a clinical trial, please inform our staff so that they may plan for your absences or find another clinical trial that may work for you.
You are free to leave or cease participation in a clinical trial at any time for any reason. Details about why you have decided to leave the study are appreciated but not mandatory. Depending on the type of clinical trial, the clinical research team may offer you advice (i.e. if a study medication needs to be withdrawn gradually), but again, this is not required.