Optimizing Outcomes of Treatment-Resistant Depression in Older Adults
NCT02960763 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 742
Last updated 2024-10-03
Summary
The purpose of this research study is to assess which antidepressants work the best in older adults who have treatment-resistant depression (TRD).
Conditions
- Treatment Resistant Depression
- Major Depressive Disorder
- Treatment-Refractory Depression
- Late Life Depression
- Geriatric Depression
Interventions
- DRUG
-
Aripiprazole Augmentation
Augment current antidepressant treatment with aripiprazole (tablets). Start at 2 mg daily; increase every two weeks (i.e., to 5, 7, 10 mg) to a maximum of 15 mg daily based on symptom severity and side effects.
- DRUG
-
Bupropion Augmentation
Augment current antidepressant treatment with bupropion once-daily extended release, starting at 150 mg daily; titrated after four weeks to 300 mg daily based on symptom severity and side effects.
- DRUG
-
Switch to bupropion
Taper from current antidepressant therapy. Start bupropion once-daily extended release at 150 mg daily; titrated after four weeks to 300 mg daily based on symptom severity and side effects.
- DRUG
-
Lithium Augmentation
Augment current antidepressant treatment with lithium carbonate tablets starting at 300 mg daily, titrated per blood level to 0.4-0.6 meQ/L.
- DRUG
-
Switch to nortriptyline
Taper from current antidepressant therapy. Start on nortriptyline tablets starting at 1 mg per kg of body weight daily, titrated per blood level to 80-120 ng/ml
Sponsors & Collaborators
-
Patient-Centered Outcomes Research Institute
collaborator OTHER -
National Institute of Mental Health (NIMH)
collaborator NIH -
Washington University School of Medicine
lead OTHER
Principal Investigators
-
Eric Lenze, MD · Washington University School of Medicine
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-02-24
- Primary Completion
- 2020-09-28
- Completion
- 2021-09-01
- FDA Drug
- Yes
Countries
- United States
- Canada
Study Locations
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