Clinical Trials Directory

Trials / Completed

CompletedNCT01386086

Aripiprazole and Resistant Postpartum Depression

Augmentation Therapy of Resistant Postpartum Depression With Aripiprazole

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
10 (actual)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Currently there are no controlled data on the management of postpartum depression that fails to respond to adequate antidepressant therapy. The investigators recently reported that a large number of patients responded to the addition of atypical neuroleptics after having failed antidepressant trials. Aripiprazole used adjunctively to antidepressants is effective in patients with resistant depression but it has not been studied in patients with resistant postpartum depression. The investigators propose to conduct a 6 week open-label study to assess the effectiveness and tolerability of aripiprazole used adjunctively to antidepressants in patients with resistant postpartum depression.

Conditions

Interventions

TypeNameDescription
DRUGaripiprazoleThe starting dose of aripiprazole will be 2 mg and the dose adjusted to a maximum of 15 daily

Timeline

Start date
2011-06-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2011-06-30
Last updated
2016-03-17

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01386086. Inclusion in this directory is not an endorsement.