Clinical Trials Directory

Trials / Completed

CompletedNCT00179244

Risperidone vs. Bupropion ER Augmentation of SSRIs in Treatment-Resistant Depression

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
30 (planned)
Sponsor
Vanderbilt University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the comparative effectiveness of Risperdal (risperidone) or bupropion ER (extended release) combined with a SSRI medication and to test the relative safety of the combinations.

Detailed description

Major depression is a severe disorder with serious consequences. Effective treatments are available; however, in clinical trials 30-40% of patients do not experience even a 50% reduction in depression severity scores, while 50-70% fail to achieve a full therapeutic response. Futhermore, impairment from the disorder continues essentially unabated in patients who are treated but do not fully remit. If anything, the situation is at least as bad or not worse in clinical practice. Clearly, alternatives are needed to manage this common clinical condition. The addition of bupropion ER (extended release) to an SSRI has empirical support, and has become the most common augmentation strategy in the US. A comparative trial of the combination of risperidone or bupropion ER added to an SSRI in treatment resistant deperssion could help support risperidone for this condition; such a trial seems warranted at this time. Patients who are currently on a SSRI at an adequate dosage for at least 3 weeks with no response, will be randomly assigned (open-label) to either risperidone or bupropion ER augmentation for a period of 6 weeks. Patients will be followed weekly at the beginning and bi-weekly towards the end of the trial to compare the response of each group.

Conditions

Interventions

TypeNameDescription
DRUGRispridone (drug) and Bupropion ER (drug)

Timeline

Start date
2004-07-01
Completion
2005-04-01
First posted
2005-09-15
Last updated
2015-06-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00179244. Inclusion in this directory is not an endorsement.