Agile Clinical Research Trial is actively recruiting volunteers for our clinical trials and research studies. We look for people afflicted with the specific condition being studied as well as healthy individuals.
Once you indicate an interest in volunteering, our physician will review your medical history and determine if you are a candidate. Each study has specific requirements for its volunteers. Clinical trial eligibility requirements may include:
Age, Sex, Type of disease, Stage of disease, Current health status, Current and past treatments.
Often certain groups such as African Americans, Hispanic Americans, Asian Americans or women are particularly needed since drugs can work differently in minorities and women.
Eligibility criteria differs from study to study. By adhering to stringent criteria, the researchers will be able obtain accurate and meaningful results. This criteria also ensures that more vulnerable individuals are not subjected to unnecessary risk.
After determining your eligibility, the clinical trial or research study will be explained to you by the physician and study coordinator and detailed in an Informed Consent document, which you will be asked to sign. Informed Consent is meant to protect your safety and rights.
You cannot participate in any clinical trial without signing the Informed Consent form. Informed Consent is not a contract and you can leave the clinical trial or research study at any time.
These medical services are provided at no charge to you. In addition, you may be compensated for your time and travel.
Once you qualify for one of our studies you will receive detailed information on the individual clinical trial. This information ensures that you are fully informed of participation requirements before deciding to participate. Your personal medical information will be handled confidentially.
Please Contact Us for further information...