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Selective Serotonin Reuptake Inhibitor
B for Depression (iSPOT-D Trial)
Phase 4
Waitlist Available
Led By Radu V Saveanu, MD
Research Sponsored by BRC Operations Pty. Ltd.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 52-weeks
Awards & highlights
iSPOT-D Trial Summary
The aim of this study is to identify genetic, physical (brain) and psychological (cognitive) markers (or combinations of them) that predict specific response to a range of antidepressants treatment (Escitalopram, Venlafaxine, Sertraline) in patients diagnosed with major depressive disorder. This study is focused on outcomes which may impact on how "personalised medicine" is implemented in depression.
Eligible Conditions
- Depression
iSPOT-D Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 52-weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~52-weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
To determine whether the genetic-brain-cognition function markers (or combination of markers) 'normalise' with acute drug treatment in MDD
Secondary outcome measures
To determine whether markers of acute treatment prediction are also predictive of functional outcome over 6-12 months.
iSPOT-D Trial Design
4Treatment groups
Active Control
Group I: BActive Control1 Intervention
Sertraline
Group II: DActive Control1 Intervention
Healthy matched controls
Group III: CActive Control1 Intervention
Venlafaxine-XR
Group IV: AActive Control1 Intervention
Escitalopram
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Who is running the clinical trial?
BRC Operations Pty. Ltd.Lead Sponsor
1 Previous Clinical Trials
1,344 Total Patients Enrolled
Radu V Saveanu, MDPrincipal InvestigatorUniversity of Miami
Anthony Harris, MDPrincipal InvestigatorBrain Dynamics Centre
Frequently Asked Questions
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