View details of current studies at KUMC CTSU Wichita:

Pediatrics

• Research database – Interested in learning more about future clinical trials? Join our research database! The purpose of this database is to collect potential participants’ demographic and personal health information to determine if they qualify for any current and/or future research studies.

Adults

• Research database – Interested in learning more about future clinical trials? Join our research database! The purpose of this database is to collect potential participants’ demographic and personal health information to determine if they qualify for any current and/or future research studies.

In partnership with KU Medical Center in Kansas City, CCR is also participating in the following clinical trials:

• Alzheimer’s Prevention – Study for adults 40-60 without memory impairment to complete surveys regarding the benefits of diet and exercise for the prevention of Alzheimer’s disease and the effects of menopause on long-term brain health. Surveys are completed online or via telephone and are expected to take 15-30 minutes to complete. Participants will receive $75 upon completion of all surveys. Learn more from the study flyer.
• ALS - Muscle cramps – The purpose of this study is to learn more about how the study drug might work to help treatment muscle cramps in individuals diagnosed with Amyotrophic Lateral Sclerosis (ALS). This study will last about 28 weeks, and participants will have up to five in-person visits to the clinic and three phone call visits during this time.
• COPD – RELIANCE is a nationwide study that compares azithromycin and roflumilast to learn if long-term use improves the lives of people with COPD. RELIANCE is looking for participants who are least 40 years of age, have been diagnosed with COPD or hospitalized for COPD in the last 12 months, and are discussing stronger COPD treatment with their doctor.
• Cohort – The Clinical Cohort Study is working to establish and maintain a group of potential research participants willing to allow us to follow their aging process over time. Participants must have a current diagnosis of dementia, Alzheimer’s disease or mild cognitive impairment. Participation in this study would require yearly visits for as long as the participant is willing and/or able. These visits will include a clinical evaluation, memory evaluation and additional optional assessments.