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Clinical trials are conducted to evaluate whether new treatment approaches offer improved outcomes and/or improved quality of life. Through the Cancer Program's relationship with the University of Pennsylvania Cancer Network, our medical, surgical and radiation oncologists at the Hospital can offer patients access to a wide range of treatment and prevention trials. Before they are offered to patients, all trials are thoroughly reviewed and approved by the Institutional Review Board, which provides oversight of clinical trials and protection of human research subjects.
Not all trials study new drugs; many test new surgical procedures and radiation therapy techniques, and some even explore complementary or alternative medicines. Participation is always voluntary and a decision to participate is best made with your entire team of caregivers as well as your family. Your doctor will discuss with you if there is a treatment clinical trial appropriate for you to consider.
The following provide details on the clinical trials at The Cancer Program of The Chester County Hospital, a member of the University of Pennsylvania Cancer Network.
The Cancer Program participates in clinical prevention trials, most notably the STAR and SELECT studies. Both the STAR and SELECT studies have completed the recruitment and enrollment phases of the study, and remain in the follow-up phase. We are recruiting to the WISER SISTER Study and The Testicular Study. The WISER SISTER Study is designed for sisters and daughters of women who have been diagnosed with breast cancer. The Testicular Study is designed to study the inherited genetic variation and predisposition of men diagnosed with testicular cancer. Please call our Reesearch Nurse at 610.431.5297 for additional information.
Institutional Review Board
The Institutional Review Board (IRB) is a multidisciplinary group of individuals designated by the authority of the Board of Directors as a committee to safeguard the rights and welfare of human subjects recruited to participate in research activities at the hospital. The IRB committee members possess varying experiences and professional competencies necessary to perform the scientific, regulatory, and ethical oversight for research activities conducted at the hospital for the protection of human research subjects.
All human subject research at the Hospital requires the review and approval by the IRB prior to initiating the activity. The purpose of the IRB review is to evaluate the ethics and methods of the research, to promote a fully informed consent process and ensure voluntary participation by prospective subjects, and to maximize the safety of the subjects once enrolled into the research study.
The IRB Coordinator will provide guidance to Hospital-affiliated members with an interest in initiating a biomedical or social science study. The Institutional Review Board will determine if the activity qualifies for IRB oversight and approval or an IRB exemption. Inquiries for human subject research guidance can contact the IRB coordinator at 610.431.5064.
Last Updated: 7/11/2012