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
| Type | Name | Description |
|---|---|---|
| OTHER | Discontinuation of serotonergic antidepressants | Discontinuation 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. |
| OTHER | Continuation of serotonergic medications | Continuation 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.