Pioglitazone and Quetiapine XR Pharmacogenetic Study
Status: | Completed |
---|---|
Conditions: | Depression, Depression, Major Depression Disorder (MDD), Psychiatric, Bipolar Disorder |
Therapuetic Areas: | Psychiatry / Psychology, Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | February 2011 |
End Date: | May 2015 |
Pharmacogenetic Study of Pioglitazone and Quetiapine XR Treatment Response in Mood Disorders
Obtain phenotypic data and a DNA/blood sample from mood disorder patients undergoing
pioglitazone or quetiapine XR treatment as a part of an IRB approved clinical trial
conducted at the Mood Disorders Program. Pioglitazone treatment is examined in metabolic
syndrome comorbid with bipolar depression (IRB # 07-08-24) and unipolar depression (IRB #
07-07-20). Quetiapine XR treatment is examined in generalized anxiety disorder comorbid with
bipolar depression (IRB # 10-06-19) and unipolar depression (IRB # 12-01-29). Please refer
to the respective IRB protocols for more information.
pioglitazone or quetiapine XR treatment as a part of an IRB approved clinical trial
conducted at the Mood Disorders Program. Pioglitazone treatment is examined in metabolic
syndrome comorbid with bipolar depression (IRB # 07-08-24) and unipolar depression (IRB #
07-07-20). Quetiapine XR treatment is examined in generalized anxiety disorder comorbid with
bipolar depression (IRB # 10-06-19) and unipolar depression (IRB # 12-01-29). Please refer
to the respective IRB protocols for more information.
Inclusion Criteria:
- 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
Exclusion Criteria:
- Patient lacks the capacity to provide informed consent
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