RecruitingPhase 4ACTRN12608000476336

International Study to Predict Optimized Treatment - in Depression

International Study to Predict Optimized Treatment response to the three most commonly used antidepressants (Escitalopram, Sertraline and Venlafaxine extended release XR,) in subjects diagnosed with major depressive disorder (MDD) as compared to matched healthy controls.


Sponsor

Brain Resource

Enrollment

2,688 participants

Start Date

Jul 15, 2008

Study Type

Interventional

Conditions


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 65 Yearss

Inclusion Criteria1

  • Meet Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV)criteria for primary Major Depressive Disorder with a Hamilton Rating Depression Scale (HAM-D) score >/= 16 and who are fluent in English or Dutch.

Exclusion Criteria4

  • Presence of suicidal ideations, biopoloar, psychosis or primary eating disorder.
  • Prior or resent use antidepressants including escitalopram, sertraline, venlafaxine XR.
  • History of brain injury/blow resulting in loss of consciousness.
  • evere impediment to vision, hearing and/or hand movement which may interfere with their ability to complete the protocol required test.

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Interventions

Once randomised and on drug, subjects will be dosed with study medication as per local/country standard of care. Therefore, the length of treatment will differ and is based on the subjects response.

Once randomised and on drug, subjects will be dosed with study medication as per local/country standard of care. Therefore, the length of treatment will differ and is based on the subjects response. escitalopram one 10 mg tablet orally once daily (QD) sertraline one 50 mg orally QD venlafaxine extended release (XR) one 75 mg orally QD


Locations(7)

Missouri, United States of America

California, United States of America

New York, United States of America

Rhode Island, United States of America

North Carolina, United States of America

Auckland, New Zealand

Nijmegen, Netherlands

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ACTRN12608000476336


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