N/A
N=104
Retrospective Analysis of Outcomes With a Pharmacogenomic Algorithm
Depression · Anxiety
Bottom Line
View on ClinicalTrials.gov: NCT01632267 ↗Enrolled (actual)
104
Serious AEs
0.0%
Results posted
Mar 2013
Primary outcome: Primary: Number of Outpatient Visits — 13 units on a scale
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Assurex Health Inc.
- Primary completion
- Apr 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Outpatient Visits |
13 | — |
| SECONDARY Number of Medical Absence Days |
— | — |
| SECONDARY Number of Disability Claims |
— | — |
Summary
Antidepressants are among the most widely prescribed medications, yet only 35-45% of patients achieve remission following an initial antidepressant trial. The financial burden of treatment failures in direct treatment costs, disability, decreased productivity, and missed work may in part derive from a mismatch between optimal, and actual, medications prescribed. The present one year retrospective study seeks to evaluate the indirect and direct healthcare costs for 96 patients with a DSM-IV-TR depressive or anxiety disorder, in relation to an interpretive reporting system designed to predict antidepressant responses based on DNA variations in cytochrome P450 genes (CYP2D6, CYP2C19, CYP1A2), the serotonin transporter gene (SLC6A4), and the serotonin 2A receptor (5HTR2A) genes.
Eligibility Criteria
Inclusion Criteria
- Major Depressive Disorder
- Dysthymic Disorder
- Depressive Disorder NOS
- Obsessive Compulsive Disorder (OCD)
- Generalized Anxiety Disorder
- Panic Disorder
- Anxiety Disorder NOS
- Post-Traumatic Stress Disorder (PTSD)
- Social Phobia
Exclusion Criteria
- Bipolar Disorder
- Schizophrenia
- Schizoaffective Disorder
- Previous pharmacogenomic testing
Data sourced from ClinicalTrials.gov (NCT01632267). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.