Evaluation of Pharmacogenetic Testing In a Mental Health Population and Economic Outcomes
Completed
Conditions studied: Major Depressive Disorder 1
In brief
This is a non-randomized, single-case design of pharmacogenetic implementation in a mental health patient population of subjects taking antipsychotics and/or antidepressants.
Key facts
- Study ID
- NCT02474680
- Run by
- Avera McKennan Hospital & University Health Center
- People needed
- 84
- Starts
- 2015-11-01
- Expected to finish
- 2017-01-01
- Last updated by the study team
- 2017-05-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Must be taking either an anti-depressant or an anti-psychotic medication
- Must provide informed consent
- Must have Avera Health Plans insurance coverage
- Must have three months of participation in the Avera Care Coordination Program
You may not qualify if…
- Must not be pregnant or breastfeeding
- Must not have an active and/or unstable diagnosis of substance abuse
- Must not have a primary diagnosis of dementia, bulimia, or anorexia nervosa disorder
- Must not have had a previous pharmacogenetic evaluation
Where it is running
- Avera Institute for Human Genetics — Sioux Falls, South Dakota, United States
Full record on ClinicalTrials.gov
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