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There are many types of clinical trials such as those studying new pain medications, diagnostic tools, and spinal implants. The United States Food and Drug Administration (FDA) is responsible for regulating clinical trials. Different organizations and individuals sponsor and/or fund clinical trials. These include doctors, medical institutions, federal agencies, and companies (implant manufacturers, diagnostic companies, pharmaceutical firms, and others).
Clinical trials follow a study plan or protocol. Think of a protocol as the rules of the clinical trial. A protocol can include information about how the study is conducted, its location, participant eligibility, how often participants are evaluated, and the duration of the study. The protocol is followed closely to help ensure participant safety and so study results can be accurately reported.
There is no cost to participate in any of our clinical trials or research studies and all information is kept strictly confidential. You can also be assured that involvement in our research studies will not affect the insurability of any family member.
To learn if you are eligible to participate in one of our clinical trials simply:
- Sign the patient consent form.
- Complete the participant questionnaire
- Provide a release for us to obtain a copy of your medical records and/or x-rays pertaining to the disease being studied.
- Provide a saliva sample.