As part of our mission to provide comprehensive and state of the art care, all IUI providers participates in clinical trials. Our research team works with some of the world’s leading pharmaceutical and medical technology companies in many phases of drug and device research. Research at IUI is conducted according to Good Clinical Practice (GCP) and in compliance with all federal regulations. Our team maintains membership and certifications through the Association of Clinical Research Professionals (ACRP).
About Clinical Trials
Every new drug and device must go through an extensive process to achieve Food and Drug Administration (FDA) approval. Phase I trials investigate the safety of a drug in a small number of healthy volunteers. In Phase II trials, the drug is tested in a small number of patients that have the diagnosis the medication is designed to treat. Phase II research helps determine a tolerable, safe and effective dose of the drug. Phase III trials involve larger numbers of patients with the condition/disease and are to further prove safety and efficacy. Phase IV trials occur post FDA approval for a variety of reasons, including addition of an indication or head to head comparisons.
Benefits of Participation
Participation in a clinical trial may have many advantages, including:
- Access to the latest treatment before it is widely available
- Compensation for your time and travel related to your research appointments
- Close monitoring of your medical condition
- Advancement of medical therapy for patients like yourself
Participation in a clinical trial may have some drawbacks as well, including:
- Treatment may not benefit your condition
- May require more frequent visits to the clinic
- Unanticipated or undesired side effects from the investigational product
Becoming a Participant
The Research Team will provide you with the informed consent form (ICF) packet for your review. The ICF provides all the details of the study, including the drug or device, risks and benefits, compensation, tests, procedures, etc. If you choose to participate, you will then be screened for the study. At this visit the Research staff and the principal investigator will conduct procedures as mandated by the study protocol. If you qualify, you will continue with study visits. You may withdraw from participation at any time.
If you are interested in learning more about Research or a particular study, please contact us via email at email@example.com or call 208-639-4938.
Joseph H. Williams, MD, CPI
Dr. Williams is our lead physician involving clinical trials. He is a board-certified urologist. Dr. Williams received his medical training in the U.S. Navy. He has the distinction of being one of few Certified Principal Investigators in the State of Idaho. He has extensive research expertise and knowledge of Good Clinical Practice (GCP) and Food and Drug Administration (FDA) regulations pertaining to Research. He serves on many boards and committees in the Treasure Valley, including the Idaho State Board of Medicine. He served as a Scout Master for the Boy Scouts for 23 years and enjoys running, backpacking, and theatre.
Karrie Crumley, BS
Email: firstname.lastname@example.org , Contact: (208) 639 4884
Karrie has been with IUI since 2020 and has worked in various departments. She obtained her Bachelor of Science from Boise State University. She became part of the Research Team in May of 2022. Along with providing patient care, Karrie is actively involved in patient recruitment and administrative duties. She was born and raised in the Treasure Valley and enjoys numerous outdoor activities along with playing with her golden retriever.
Stephanie Luckie, BS
Email: SLuckie@idurology.com , Contact: (208) 639-4938
Stephanie has been with IUI since 2018. She has worked in several departments throughout IUI. She obtained her Bachelor of Science of Boise State University and has been involved in healthcare since 2016. She became part of the Research Team in 2020. Along with providing patient care, Stephanie is actively involved in patient recruitment and administrative duties. Born and raised in the Treasure Valley, Stephanie enjoys many outdoor activities such as hiking, fishing, and backpacking. She also enjoys learning about her Basque culture and being involved with the local Basque community.
Brian Mihm, LPN
Email: email@example.com , Contact: (208) 639-4938
Brian obtained his LPN in 2009, and soon after joined IUI/SCI in 2010. During his first 9 months with IUI, Brian worked as a float nurse. With his technology and medical background, he was then chosen to be the Information Technology Specialist, a position he held for over 12 years. In December 2022, Brian was promoted to Clinical Research Coordinator with the IUI Research Department. Prior to working at IUI/SCI, Brian worked at Micron Technology for 8 years in a production and information technology environment. He also served in the Idaho National Guard. Brian was raised in Moreland, Idaho. He and his son spend their time exploring Idaho and enjoying the great outdoors.