Status:

TERMINATED

MRS and Medication Response: A Pilot Study

Lead Sponsor:

Stanford University

Conditions:

Major Depressive Disorder

Major Depressive Episode

Eligibility:

All Genders

21-75 years

Brief Summary

We hope to demonstrate that magnetic resonance spectroscopy can detect brain concentration levels of paroxetine (Paxil) or citalopram (Celexa) or escitalopram (Lexapro) in depressed patients.

Detailed Description

The primary objective of this study is to demonstrate that it is feasible to image paroxetine (Paxil) or citalopram (Celexa) or escitalopram (Lexapro) brain concentrations using MRS technology in depr...

Eligibility Criteria

Inclusion

  • Major depressive disorder:
  • Inclusion Criteria:
  • DSM diagnosis of Major Depressive Disorder
  • Taking paroxetine \[(Paxil) or citalopram (Celexa) or escitalopram (Lexapro)\]for at least 6 weeks
  • Between 21 - 75 years of age.
  • Taking a stable dose of paroxetine \[(Paxil) or citalopram (Celexa) or escitalopram (Lexapro)\] for at least the 2 weeks prior to the imaging session
  • Healthy controls:
  • Between 21 - 75 years of age.
  • Have a 21-item HAM-D score of less than or equal to 5.
  • No current, or history of any Axis I disorder.
  • Identify exclusion criteria.
  • Exclusion criteria are as follows:
  • Contraindications for an MRI exam. These includes biomedical devices such as pacemakers, aneurysm clips, prostheses, and other metallic objects embedded in the body such as bullets, buckshot, shrapnel, and any metal fragments from working around metal.
  • Current pregnancy or lactation.
  • Patients with claustrophobia.
  • History, or current Axis I or Axis II disorders
  • Active unstable medical problems, as confirmed by screening procedures
  • Diagnosed with any autoimmune disease, (e.g., rheumatoid arthritis, Lupus, MLS).
  • Chronic use of steroids or opiates.
  • Positive urine toxicology screen for illicit substances of abuse.

Exclusion

    Key Trial Info

    Start Date :

    August 6 2013

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    August 31 2020

    Estimated Enrollment :

    3 Patients enrolled

    Trial Details

    Trial ID

    NCT03254342

    Start Date

    August 6 2013

    End Date

    August 31 2020

    Last Update

    August 19 2021

    Active Locations (1)

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    Stanford University Psychiatry and Biobehavioral Sciences

    Stanford, California, United States, 94305

    MRS and Medication Response: A Pilot Study | DecenTrialz