Clinical Trials Directory

Trials / Completed

CompletedNCT00519428

Does Dual Therapy Hasten Antidepressant Response?

Combining Antidepressants to Hasten Remission From Depression

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
245 (actual)
Sponsor
New York State Psychiatric Institute · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study will utilize a randomized double-blind design to evaluate whether initial treatment with two anti-depressant medications (escitalopram and bupropion) results in more rapid remission and greater over-all remission rates than either monotherapy in 240 depressed subjects.

Detailed description

Depression is a major public health problem due to its prevalence and accompanying dysfunction and costs. Depression is undertreated, but even when treatment is adequate and effective, sources of delay in current pharmacologic strategies include: mechanistic delays, those related to the physiologic and behavioral effects of antidepressants; dosing delays in identifying the effective dose; and programmatic delays in identifying an effective agent using sequential monotherapy. This study will randomize 240 patients with Diagnostic and Statistical Manual, 4th Edition (DSM-IV) Major Depressive Disorder (MDD) to 12 week double blind treatment with combined escitalopram and bupropion or each antidepressant administered alone to evaluate whether combined escitalopram and bupropion result in more rapid remission and greater over-all remission than monotherapy. Preclinical and clinical studies suggest that bupropion might prevent one mechanistic delay inherent in escitalopram monotherapy. Rapid dose escalation may counter dosing delays. The simultaneous use of two known antidepressant medications may alleviate programmatic delays inherent in usual sequential monotherapy. Six months follow up and careful assessment of adverse events will address tolerability, acceptability, sustainability, and pharmacoeconomic concerns. If successful, this study might have a significant impact on clinical practice, public health, and depression's cost consequences.

Conditions

Interventions

TypeNameDescription
DRUGescitalopram10mg/d increasing by 10 mg/week to a maximum of 40 mg/d if tolerated and not remitted
DRUGbupropion extra long (XL)150mg/d increasing to 300 mg/d after 1 week and 450 mg/d after 3 weeks, all increases if tolerated and not remitted
DRUGescitalopram + bupropionsame dosing schedule as for monotherapy

Timeline

Start date
2007-08-01
Primary completion
2011-07-01
Completion
2012-03-01
First posted
2007-08-22
Last updated
2017-10-04
Results posted
2017-10-04

Locations

2 sites across 2 countries: United States, Canada

Source: ClinicalTrials.gov record NCT00519428. Inclusion in this directory is not an endorsement.