Trials / Completed
CompletedNCT02544607
Ketamine for Depression: An MRI Study
Baseline Insular Dysfunction as a Predictor of Ketamine's Antidepressant Effects in Anxious Depression
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 25 (actual)
- Sponsor
- Massachusetts General Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 64 Years
- Healthy volunteers
- Accepted
Summary
Ketamine has been shown to decrease symptoms of anxious depression quickly. This decrease has been shown to last for up to one month. MRI technology will be used before and after ketamine for patients with depression to examine the extent to which certain brain areas predict ketamine's antidepressant effects.
Detailed description
Ketamine's antidepressant effects were measured with Hamilton Depression Rating Scale (HDRS). MRI data will also be analyzed to examine the extent to which certain brain areas predict ketamine's antidepressant effects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ketamine | Ketamine 0.5mg/kg over 40 minutes IV |
| OTHER | Magnetic Resonance Imaging (MRI) | MRI technology will be used before and after ketamine for patients with depression |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2017-12-29
- Completion
- 2017-12-29
- First posted
- 2015-09-09
- Last updated
- 2019-04-16
- Results posted
- 2019-04-04
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT02544607. Inclusion in this directory is not an endorsement.