Clinical Trials Directory

Trials / Unknown

UnknownNCT03786614

Antidepressant Discontinuation in Treatment Resistant Depression

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
University of Louisville · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effects on depressive symptoms of subjects who discontinue serotonergic antidepressants (a certain type of antidepressant, such as Prozac, that works on serotonin receptors in the brain) with the effects on depressive symptoms of subjects who continue to take serotonergic antidepressants. During this study, subjects will also be presented with the opportunity to undergo genetic testing for the serotonin gene transporter which has a short or long form. This is being done because it has been demonstrated that genetic testing improves outcome while treating treatment-resistant depression.

Conditions

Interventions

TypeNameDescription
OTHERDiscontinuation of serotonergic antidepressantsDiscontinuation of serotonergic antidepressants and possibly shift to other antidepressant categories that were proven to be effective in treating depression such as pramipexole, bupropion, quetiapine, lurasidone, brexpipazole. Additionally, subjects will have access to other treatment measures of treating treatment resistant depression.
OTHERContinuation of serotonergic medicationsContinuation of serotonergic medications which is the standard care of treatment. Additionally, subjects will have access to other treatment measures of treating treatment resistant depression.

Timeline

Start date
2019-06-20
Primary completion
2024-12-01
Completion
2024-12-01
First posted
2018-12-26
Last updated
2023-08-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03786614. Inclusion in this directory is not an endorsement.