Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University Hospitals Cleveland Medical Center
With
National Institutes of Health (NIH)
National Center for Research Resources (NCRR)
Age
18–70
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Must have participated in IRB protocols 10-06-19, 12-07-29, 07-07-20, and 07-08-24
Patient must give consent to participate, sign and date the IRB approved written informed consent form prior to the initiation of any procedures for this study
Patient must be diagnosed with Bipolar Disorder or Major Depressive Disorder
Patient must be at least 18 years old
Patient must be willing to give a blood sample
You may not be if
Patient lacks the capacity to provide informed consent
Clareo Health | Pioglitazone and Quetiapine XR Pharmacogenetic Study
