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Selective Serotonin Reuptake Inhibitor
2 for Depression
Phase 4
Waitlist Available
Led By Mark J Rapoport, MD, FRCPC
Research Sponsored by Ontario Neurotrauma Foundation
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 40 weeks
Awards & highlights
Study Summary
The purpose of the study is to explore to what extent continuing the antidepressant medication citalopram (Celexa), after depression has responded to treatment, helps prevent the return of depressive symptoms in patients with recent traumatic brain injury (TBI).
Eligible Conditions
- Depression
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 40 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~40 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
recurrence of major depression by administering the Hamilton Depression Rating Scale (HAM-D) and Clinical Global Impressions Scale (CGI) every 4 weeks for 40 weeks
Secondary outcome measures
general cognitive function at baseline, 10 weeks and on termination of the trial
list of adverse drug events at baseline, 10 weeks and on termination of the trial
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: 2Experimental Treatment1 Intervention
Group II: 1Placebo Group1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Citalopram
FDA approved
Find a Location
Who is running the clinical trial?
Ontario Neurotrauma FoundationLead Sponsor
22 Previous Clinical Trials
1,082 Total Patients Enrolled
3 Trials studying Depression
200 Patients Enrolled for Depression
Mark J Rapoport, MD, FRCPCPrincipal InvestigatorSunnybrook Health Sciences Centre, University of Toronto
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