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Antidepressant Maintenance in Traumatic Brain Injury

Primary Purpose

Depression

Status
Unknown status
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
citalopram
Placebo
Sponsored by
Ontario Neurotrauma Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Traumatic Brain Injury, Depression, Antidepressant medication, Double-Blind Study, Brain Injuries, Antidepressive Agents, Citalopram, Double-Blind Method

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age > 18 years TBI within the last year (this is consistent with clinic population) Mild TBI Written, informed consent Diagnosis of major depressive episode using the depression module of the Structured Clinical Interview for DSM-IV Axis I disorders (SCID-IV), and baseline 17-item Hamilton Depression (HAM-D) Rating Scale score of 16 and above (prior to selective serotonin reuptake inhibitor [SSRI] treatment) Response to citalopram 20 or 40mg/d, as defined as a reduction in baseline HAM-D of >= 50%, and HAM-D score of 10 or below; or response to citalopram defined as not meeting DSM-IV criteria for major depression and Clinical Global Impression - severity of mildly ill, borderline ill, or normal and a Clinical Global Impression - improvement of much improved or very much improved impression. Exclusion Criteria: Prior TBI or other focal brain disease (e.g., stroke, tumour) Significant acute medical illness including: drug overdose; severely disturbed liver, kidney, lung or heart function; anemia; hypothyroidism; uncontrolled diabetes; Parkinson's disease; Huntington's chorea; progressive supranuclear palsy; brain tumor; subdural hematoma; or multiple sclerosis. Current alcohol or substance abuse A brain computed tomographic (CT) scan revealing focal lesions that could not be interpreted as consistent with TBI Presence of premorbid psychiatric diagnosis of schizophrenia, dementia or bipolar disorder Prior episode of major depression in two years prior to TBI, based on SCID-IV interview Prior treatment with citalopram or contraindications to receiving treatment with citalopram

Sites / Locations

  • Sunnybrook Health Sciences Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

1

2

Arm Description

Outcomes

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

Full Information

First Posted
September 10, 2005
Last Updated
June 3, 2008
Sponsor
Ontario Neurotrauma Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00162916
Brief Title
Antidepressant Maintenance in Traumatic Brain Injury
Official Title
A Randomized Controlled Trial of Antidepressant Maintenance for Major Depression Following Mild Traumatic Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
June 2008
Overall Recruitment Status
Unknown status
Study Start Date
May 2005 (undefined)
Primary Completion Date
May 2008 (Actual)
Study Completion Date
October 2008 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Ontario Neurotrauma Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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).
Detailed Description
While antidepressants are effective in treating major depression following TBI, there is a lack of certainty as to how long antidepressants must be continued following improvement of symptoms. Many studies published in the last decade strongly show that antidepressants prevent relapse in patients with major depression in the absence of traumatic brain injury (TBI). However, is it unknown as to whether this is the case following TBI. The aim of this study is to determine whether being on an antidepressant for a year reduces the risk of relapse of depression. Patients diagnosed with major depression following mild TBI will be treated for ten weeks with the antidepressant drug citalopram. Those who respond, meaning that the symptoms of depression have lessened significantly, will be randomly assigned to either continue taking the citalopram for one year or to take a placebo for one year. Every four weeks, for an additional forty weeks, patients will be assessed for relapse of depression. This study will have a double-blind design, meaning that neither patient nor clinician know whether citalopram or placebo is being administered. The primary outcome of interest will be a comparison of the percentage of patients who have a recurrence of major depression while continued on citalopram compared with those who were switched to placebo after the acute phase. Recurrence will be defined as meeting Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) criteria for major depression and a Hamilton Depression Scale (HAM-D) score of > 16. Or meeting DSM-IV criteria for major depression and having a Clinical Global Impression (CGI) severity score of >= 4 and a CGI illness score of >= 3. The HAM-D and CGI will be administered every four weeks for forty weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
Keywords
Traumatic Brain Injury, Depression, Antidepressant medication, Double-Blind Study, Brain Injuries, Antidepressive Agents, Citalopram, Double-Blind Method

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Placebo Comparator
Arm Title
2
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
citalopram
Other Intervention Name(s)
Celexa
Intervention Description
20mg or 40mg, once daily, for 40 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Cornstarch
Primary Outcome Measure Information:
Title
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
Time Frame
40 weeks
Secondary Outcome Measure Information:
Title
general cognitive function at baseline, 10 weeks and on termination of the trial
Time Frame
40 weeks
Title
list of adverse drug events at baseline, 10 weeks and on termination of the trial
Time Frame
40 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years TBI within the last year (this is consistent with clinic population) Mild TBI Written, informed consent Diagnosis of major depressive episode using the depression module of the Structured Clinical Interview for DSM-IV Axis I disorders (SCID-IV), and baseline 17-item Hamilton Depression (HAM-D) Rating Scale score of 16 and above (prior to selective serotonin reuptake inhibitor [SSRI] treatment) Response to citalopram 20 or 40mg/d, as defined as a reduction in baseline HAM-D of >= 50%, and HAM-D score of 10 or below; or response to citalopram defined as not meeting DSM-IV criteria for major depression and Clinical Global Impression - severity of mildly ill, borderline ill, or normal and a Clinical Global Impression - improvement of much improved or very much improved impression. Exclusion Criteria: Prior TBI or other focal brain disease (e.g., stroke, tumour) Significant acute medical illness including: drug overdose; severely disturbed liver, kidney, lung or heart function; anemia; hypothyroidism; uncontrolled diabetes; Parkinson's disease; Huntington's chorea; progressive supranuclear palsy; brain tumor; subdural hematoma; or multiple sclerosis. Current alcohol or substance abuse A brain computed tomographic (CT) scan revealing focal lesions that could not be interpreted as consistent with TBI Presence of premorbid psychiatric diagnosis of schizophrenia, dementia or bipolar disorder Prior episode of major depression in two years prior to TBI, based on SCID-IV interview Prior treatment with citalopram or contraindications to receiving treatment with citalopram
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark J Rapoport, MD, FRCPC
Organizational Affiliation
Sunnybrook Health Sciences Centre, University of Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
20441723
Citation
Rapoport MJ, Mitchell RA, McCullagh S, Herrmann N, Chan F, Kiss A, Feinstein A, Lanctot KL. A randomized controlled trial of antidepressant continuation for major depression following traumatic brain injury. J Clin Psychiatry. 2010 Sep;71(9):1125-30. doi: 10.4088/JCP.09m05086blu. Epub 2010 Apr 20.
Results Reference
derived

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Antidepressant Maintenance in Traumatic Brain Injury

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