Screening trials

The coordinator and the investigator will provide you with information about the trial and answer any questions you may have. The investigator will then continue the screening process. The series of assessments required depends on the clinical trial protocol. Often required is a physical examination e. Here are some examples:. Laboratory testing e. This will, however, require you to provide informed consent first. The information sheet and form will provide you with important information about the trial.

The form can be taken home to discuss with family, friends or other doctors and signed upon returning to the trial site if you decide to participate in the trial.

Note: This document is not a contract, it represents an agreement to participate in the trial and an understanding of what it will involve. You may withdraw your consent and leave the trial at any time. Complex Regional Pain Syndrome Awareness. Clinical Trials — The Role of the Coordinator. GRS Newsletter — August GRS Newsletter — December Email: reception genesisresearchservices. Disclaimer: This website provides general information only; it should not be construed as medical advice nor does it replace the need to seek medical advice from a qualified medical professional.

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Questions to Ask about Advanced Cancer. Managing Cancer Care. Finding Health Care Services. Advance Directives. Using Trusted Resources. Adolescents and Young Adults with Cancer. Emotional Support for Young People with Cancer. Cancers by Body Location. Late Effects of Childhood Cancer Treatment.

Pediatric Supportive Care. Rare Cancers of Childhood Treatment. Childhood Cancer Genomics. Study Findings. Metastatic Cancer Research. Intramural Research. Extramural Research. Cancer Research Workforce. Partners in Cancer Research. What Are Cancer Research Studies. Research Studies. Get Involved. Cancer Biology Research. Cancer Genomics Research. Research on Causes of Cancer. Cancer Prevention Research.