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Clinical Trials
Ellis Fischel The Ellis Fischel Cancer Center Clinical Trials Office is a repository for all clinical research at Ellis Fischel. This includes national cooperative group studies, such as Cancer and Leukemia Group B (CALGB), National Surgical Adjuvant Breast and Bowel (NSABP), Gynecology Oncology Group (GOG), and Radiation Therapy Oncology Group (RTOG), pharmaceutical studies, and in-house studies. Services provided by this centralized clinical research office include data management, IRB application submission, grant submission, and nursing support.
University Hospital The University of Missouri Health Care is home to many dedicated and experienced researchers. Together with coordinators and other support staff, our researchers form an effective research team dedicated to Discovering tomorrow’s health care today……… The Health Sciences Center has conducted clinical trials for more than 40 years. Many of these trials have resulted in approval of new drugs from the Food and Drug Administration. The broad experience of our research team combined with our wide range of clinical opportunities makes the center an attractive site for conducting clinical research. Volunteers help speed future improvements in medical care to those in need. The University of Missouri Health Care has a broad base of clinical trial opportunities available to volunteers such as you.
If you are interested in being a part of a clinical trial, please complete a questionnaire. This information will be maintained in a database and linked to current clinical trials or used to match you to upcoming trials. This will not be linked to your medical record. THIS IS VOLUNTARY. If you do not wish your information to be kept, notify the Office of Clinical Research and it will be removed. After you have submitted the questionnaire, an Office of Clinical Research coordinator will contact you for further information and answer any questions that you might have. If it is found that you may be eligible for a clinical trial, a visit with the staff will be arranged. At this time, additional details regarding the study will be shared with you. Participation is completely voluntary and you will be provided with an opportunity to review the informed consent and ask questions before you decide to participate in a trial. Any information provided will be kept confidential and maintained in a secure environment.
