Discontinuation Study Of Citalopram (Antidepressant) in Depressed Adolescents
- Conditions
- Major Depression
- Registration Number
- NCT00249886
- Lead Sponsor
- Sunnybrook Health Sciences Centre
- Brief Summary
The purpose of the study is to evaluate whether it is advantageous for adolescents who have recovered from depression after a 6 to 12 week course of antidepressant treatment to stay on the treatment a further 6 months or is it just as helpful to stop the medication after recovery.
The hypothesis is that adolescents with major depression who recover from the 6 to 12 week trial of citalopram will be less likely to have a recurrence of depression over a 6 month period if continued on the citalopram as compared to those who discontinue the medication.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- 60
- Diagnosis of major Depression.
- Age 13-18.
- A score of > 16 on the 17 item Hamilton Depression Scale or a score of > 12 on the 17 items plus a score of >7 on the atypical items.
- Males and females.
- Outpatient at initiation of double blind treatment phase.
- Ability to give informed consent.
- Past or current hypomanic or manic episode.
- Currently meets criteria for a Conduct Disorder.
- Current psychotic symptoms.
- Substance dependence in the last 3 months.
- Significant medical condition that would contraindicate the use of an antidepressant.
- Pregnancy
- Past treatment with Citalopram for major depression
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Relapse - subject meets criteria for an episode of major depression for 2 weeks or more.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Sunnybrook Health Sciences Centre
🇨🇦Toronto, Ontario, Canada