Trials / Completed
CompletedNCT00253266
Venlafaxine Augmentation in Treatment Resistant Depression
Comparison of Venlafaxine Augmentation With Quetiapine v.s. Placebo in Treatment Resistant Depression
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 126 (actual)
- Sponsor
- Max-Planck-Institute of Psychiatry · Academic / Other
- Sex
- All
- Age
- 20 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
This is an assessment of the efficacy of venlafaxine-HCL augmentation with the neuroleptic quetiapine in treatment resistant depression.
Detailed description
We examine the efficacy of Venlafaxine-HCL augmentation with the neuroleptic Quetiapine in treatment resistant depression in a double-blind randomized clinical trial. Secondary objective is the evaluation of pharmacogenetic factors contributing to drug efficacy in treatment resistant depression.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Venlafaxine | Venlafaxine XR up to 450 mg/d during the complete trial (8 weeks) |
| DRUG | Quetiapine | Quetiapine up to 200 mg/d for four weeks |
Timeline
- Start date
- 2008-04-01
- Primary completion
- 2014-04-01
- Completion
- 2014-08-01
- First posted
- 2005-11-15
- Last updated
- 2015-04-08
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT00253266. Inclusion in this directory is not an endorsement.