What a Study Participant May Expect
Who May Participate
Each pharmaceutical study has a set of guidelines about who can participate in each study. The criteria for inclusion in a study are based on such factors as age, gender, the type and stage of the disease or condition, previous treatment and other medical considerations. Remington-Davis study coordinators are trained to look for patients that fit the requirements of the various studies that we run at any given time.
Informed Consent
Once a doctor determines that you or your loved one meets the requirements for a particular study, a Remington-Davis study coordinator will explain to you why the study is being done and what you can expect. The doctor will also answer any questions you may have.
You will be given information regarding who will see your medical records and how your confidentiality is maintained.
You will be given a consent form to review and sign. Before you sign the form, you should ask questions about any part of the study or your care that you do not understand or for which you need clarification. If you decide to participate in the study, you will sign the form. Participation in clinical research is
completely voluntary. You may choose to withdraw from the study at any time.
Standard of Care
As a study participant, you will be under the care of one of the “Principal Investigators” of the clinical trial, who will be assisted by the Remington-Davis study coordinators. The Principal Investigator and the study coordinators have been certified by the pharmaceutical company and have been trained for what to expect in the patient’s condition.
As a study participant you may experience more tests and doctor visits than you would normally for your illness or condition.
Benefits to Patient
Some, but not all, pharmaceutical companies provide free therapies for patients participating in clinical trials. There is no guarantee that participating in a study will benefit you directly.
Risks
The nature and purpose of clinical research is to determine efficacy, side effects, and safety of a particular compound. Participation in a clinical trial has risk associated with it. Ask a Remington-Davis study coordinator for more information about a particular study.