FAQ’s

PARTICIPATION
Why should I volunteer for a clinical research trial?

Participation in clinical trials can possibly benefit you and help many others. A new medication or procedure can possibly reduce and/or improve symptoms or perhaps, even offer a cure for an illness. Clinical research is essential in order to discover new and better ways to treat diseases and disorders.

Most studies also provide study related medical care, study medication and any required lab work or testing at no charge. Additionally, we have a staff of dietitians that can provide dietary and nutritional advice at no charge. Compensation for your time and travel for participating in a study may also be provided.

For more information about our studies, or to be considered for participation, please e-mail us or contact COR Clinical Research at (405) 272-8481. All inquiries will be CONFIDENTIAL!

FREQUENTLY ASKED QUESTIONS

A clinical research trial is a closely controlled, medically supervised research study to determine the safety and effectiveness of a medication, medical treatment, or device. Clinical trials are an important step in making new medications available for you and future generations.

The patients relationship with their physician or primary care provider will continue during the clinical research trial process. Patients that enter a clinical research trial will only receive care related to the study for a fixed period of time.

To help you decide whether or not to participate, Dr. Corder and our research staff involved in the trial will fully explain the details of the study. This process of learning key facts about a clinical research trial before deciding whether or not to participate is known as informed consent. Informed consent is not a binding agreement, and a patient has the option to withdraw from the clinical trial at any time.


The safety and best interest of our patients is our primary concern. All clinical trial patients receive a great deal of medical attention from our staff. The FDA is responsible in regulating the safety and effectiveness of investigational medications.

The patients relationship with their physician or primary care provider will continue during the clinical research trial process. Patients that enter a clinical research trial are also encouraged to inform their primary physician of their research study involvement.

 


Each study has specific requirements such as medical condition, age and sex. A Physician will review each person’s medical history and determine if he/she meets the clinical criteria for participation.


There is no fee to participate in a study. All study related exams, study medications and lab tests are at no charge to you. In fact, most studies allow compensation for your time and travel for being in the study.


We have a dedicated research staff consisting of physicians, dieticians and nurses. Any research study requiring special testing or procedures is outsourced to highly qualified, board-certified physicians. All of our medical staff is trained with good clinical practice in mind. We also attend sponsored training programs under FDA guidelines to further our knowledge of clinical trials.