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Retrospective Analysis of Outcomes With a Pharmacogenomic Algorithm (UHS)

A

Assurex Health

Status

Completed

Conditions

Depression
Anxiety

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

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.

Enrollment

104 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

104 participants in 1 patient group

Depression and anxiety
Description:
Subjects with a primary diagnosis of depression or anxiety disorder.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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