Overview
Intranasal Ketamine for Late-Life Depression and Suicidal Ideation
Status:
Withdrawn
Withdrawn
Trial end date:
2015-07-01
2015-07-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The investigators of this study plan to investigate the feasibility and efficacy of repeated doses of intranasal ketamine in severely depressed patients who are at least 65 years of age and experiencing suicidal ideation. The results of the study could lead to development of new strategies for treating depression.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Massachusetts General HospitalTreatments:
Ketamine
Criteria
Inclusion Criteria:1) be ≥65 years old, 2) provide written informed consent, 3) meet criteria for a primary
psychiatric diagnosis of major depressive disorder according to the Structured Clinical
Interview for DSM-IV (SCID) and have a HDRS28 total score ≥20; depression may have started
at any time point in their life, and certain co-morbid diagnoses (e.g., anxiety disorders)
will be allowed insofar as they are not the primary psychiatric diagnosis, 4) have a
history of ≥2 failed medication trials during the current episode (per the Massachusetts
General Hospital Antidepressant Treatment History Questionnaire; MGH ATRQ), 5) endorse
suicidal ideation for more than 2 months, per the Columbia Suicide Severity Rating Scale
(C-SSRS) and have a HDRS28 suicide item score ≥1 (thoughts that life isn't worth living),
6) be on a stable antidepressant regimen for ≥14 days prior to Study Phase II, 7) maintain
a treating psychiatrist who is in agreement with study participation, and 8) have a
reliable chaperone accompany them home following the completion of the intranasal
administration.
Exclusion Criteria:
- Patients will be excluded if any of the following criteria are met: 1) Delirium or
dementia diagnosis, 2) unstable medical illness, 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, 4) history of multiple
adverse drug reactions, 5) current/past history of psychotic disorders or
homicidality, 6) active substance use disorders (except nicotine and caffeine) within
the past six months, positive urine toxicology screen, or past history of ketamine
abuse, 7) requirement of excluded medications (narcotics, barbiturates, theophylline,
or St. John's Wort), or 8) concurrent or recent participation in other research
studies.