Physiological and Cognitive Biomarkers for Ketamine's Antidepressant Effects
Status: | Terminated |
---|---|
Conditions: | Depression |
Therapuetic Areas: | Psychiatry / Psychology |
Healthy: | No |
Age Range: | 18 - 64 |
Updated: | 4/25/2018 |
Start Date: | July 2016 |
End Date: | February 2017 |
Anxious depression is a particularly difficult-to-treat subtype of depression. Patients with
anxious depression do not respond as well to currently available antidepressant medications.
Nevertheless, in previous studies, low dose IV ketamine, which rapidly decreases symptoms of
depression within hours in many patients with "treatment-resistant" depression, has been
associated with superior efficacy in those individuals with anxious compared with non-anxious
depression. In order to understand this unique effect more fully, the current protocol is
aimed at further delineating biomarkers of ketamine's effects among individuals with
treatment-resistant anxious depression compared to those with nonanxious depression.
anxious depression do not respond as well to currently available antidepressant medications.
Nevertheless, in previous studies, low dose IV ketamine, which rapidly decreases symptoms of
depression within hours in many patients with "treatment-resistant" depression, has been
associated with superior efficacy in those individuals with anxious compared with non-anxious
depression. In order to understand this unique effect more fully, the current protocol is
aimed at further delineating biomarkers of ketamine's effects among individuals with
treatment-resistant anxious depression compared to those with nonanxious depression.
Inclusion Criteria:
1. be 18-64 years old,
2. read, understand, and provide written informed consent in English,
3. meet criteria for a primary psychiatric diagnosis of Major Depressive Disorder (MDD)
for ≥ 4 weeks,
4. have a history ≥1 failed medication trial during the current depression,
5. be on a stable adequate dose of an FDA-approved antidepressant medication for ≥28
days,
6. maintain a treating doctor who is in agreement with study participation,
7. have a reliable chaperone to accompany them home following the completion of the
ketamine infusion day,
8. be generally healthy, as assessed by medical history, physical examination (including
vital signs), clinical laboratory evaluations, and electrocardiogram (EKG),
9. be of non-childbearing potential or use of an acceptable form of birth control
(females only).
Exclusion Criteria:
1. delirium or dementia diagnosis,
2. unstable medical illness or clinically significant laboratory results,
3. history of clinically significant cardiovascular disease or electrocardiogram (EKG)
findings, or medical conditions that put the patient at risk for possible cardiac side
effects (e.g., requirement of cardiac pacemaker) or alter brain morphology (e.g.,
recent head trauma, post intracranial surgery, intracranial mass or bleed or unstable
sleep apnea), or a blood pressure >140/95 mmHg at Screening,
4. history of multiple adverse drug reactions,
5. current/past history of psychotic disorders, history of out-of-body feelings or
derealization,
6. active substance use disorders (except nicotine and caffeine) within the past six
months or past history of ketamine/PCP (phencyclidine) abuse (we will confirm this
with collateral information from their doctor if necessary),
7. requirement of excluded medications that may interact with ketamine,
8. caffeine or nicotine use within 1 hour of psychophysiology testing, or alcohol use
within 1 day of testing,
9. pregnancy, breastfeeding, or unacceptable means of birth control (females only)
10. clinically significant hearing impairment,
11. current serious suicidal or homicidal risk,
12. concurrent participation in other research studies involving medications or other
treatments,
13. narrow angle glaucoma,
14. acute intermittent porphyria history,
15. history of seizures in the past 6 months, regardless of seizure type,
16. hyperthyroidism or untreated hypothyroidism,
17. airway instability or pulmonary disease with hypercarbia, or
18. current or past cubital or carpal tunnel syndrome.
We found this trial at
1
site
185 Cambridge Street
Boston, Massachusetts 02114
Boston, Massachusetts 02114
617-724-5200
Phone: 617-726-8895
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