Formerly Ormond Medical Arts Complete Health™ Solutions for You and Your Family Please contact us to schedule an appointment or to learn more about our services. We offer early hours to fit your schedule and walk-ins are always welcome. Patient Portal Accepted Insurance Call for an appointment 386-677-0453 Set as my default Location
Ormond Beach, FL 32174 Find on map HOURS Monday – Friday: 6:00 a.m. - 5:00 p.m. PHONE 386-677-0453 FAX 386-677-0463 Call us Providers David Carpenter, MD Family Practice Sandford Kinne, III, DO
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An informed consent is a process in which the participant learns the key facts about the trial before deciding to participate or not. To help with this decision, the doctor and/or nurse explain the details of the trial. These details include the purpose, duration, requirements and key contacts.
In some circumstances, the IRB overseeing the research and the sponsor or contract research organization coordinating the trial will also have access to personal information.
The factors that allow volunteers to participate in a clinical trial are called "inclusion criteria" and the factors that disallow volunteers from participating are called "exclusion criteria.". These criteria can include age, gender, the type and stage of a disease, previous treatment history, and other medical conditions.
The volunteers' health will continue to be monitored during and after the trial.
The participant, physician, and research staff may not know which volunteer receives a placebo and which receives the active treatment. Not knowing which participants are receiving the active treatment allows the physician and research staff to objectively observe the volunteers during the study.