Ketamine for Suicidality in Bipolar Depression
Primary Purpose
Bipolar Disorder, Major Depressive Episode, Suicidal Ideation
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Ketamine
Midazolam
Sponsored by
About this trial
This is an interventional treatment trial for Bipolar Disorder focused on measuring Ketamine, Midazolam, Bipolar Disorder, Major Depressive Episode, Suicidal Ideation, Suicide, Depression, Treatment, Ketamine Treatment
Eligibility Criteria
INCLUSION CRITERIA:
- Bipolar depression with current major depressive episode (MDE). Participants may be psychiatric medication-free, or if on psychiatric medication, not responding adequately given current MDE with suicidal ideation.
- Moderate to severe suicidal ideation
- 18-65 years old
- Patients will only be enrolled if they agree to voluntary admission to an inpatient research unit at the New York State Psychiatric Institute (NYSPI) for infusion phase of treatment.
- Pre-menopausal female participants of child-bearing potential must be willing to use an acceptable form of birth control during study participation such as condoms, diaphragm, oral contraceptive pills
- Able to provide informed consent
- Subjects 61-65 years old must score 25 or higher on the Mini-Mental State Examination (MMSE) at screening
EXCLUSION CRITERIA:
- Unstable medical condition or neurological illness, including baseline hypertension (BP>140/90) or significant history of cardiovascular illness
- Significant ECG abnormality
- Pregnancy and/or lactation
- Current psychotic symptoms
- Contraindication to any study treatment
- Current or past ketamine abuse or dependence ever (lifetime); any other drug or alcohol dependence within past 6 months; suicidality only due to binge substance use or withdrawal
- Inadequate understanding of English
- Prior ineffective trial of or adverse reaction to ketamine or midazolam
- Opiate use greater than total daily dose of 20mg Oxycodone or equivalent during the 3 days pre-infusion
Sites / Locations
- Columbia University/New York State Psychiatric Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Ketamine
Midazolam
Arm Description
0.5 mg/kg, I.V. (in the vein)
0.02 mg/kg, I.V. (in the vein)
Outcomes
Primary Outcome Measures
Change in Suicidal Ideation Measured With the Beck Scale for Suicidal Ideation
Change in suicidal ideation in Bipolar Disorder during a Major Depressive Episode (MDE), with moderate to severe suicidal thoughts, from the pre-infusion baseline to 24 hours after the infusion of Ketamine (study drug) or Midazolam (active control).
Secondary Outcome Measures
Change in Systolic Blood Pressure
Blood pressure is measured in millimeters of mercury.
Full Information
NCT ID
NCT01944293
First Posted
September 8, 2013
Last Updated
February 27, 2020
Sponsor
New York State Psychiatric Institute
Collaborators
Brain & Behavior Research Foundation
1. Study Identification
Unique Protocol Identification Number
NCT01944293
Brief Title
Ketamine for Suicidality in Bipolar Depression
Official Title
Ketamine vs. Midazolam in Bipolar Depression
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
September 2017 (Actual)
Study Completion Date
October 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
New York State Psychiatric Institute
Collaborators
Brain & Behavior Research Foundation
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is designed to compare the effectiveness of two medications, Ketamine and Midazolam, for rapidly relieving suicidal thoughts in people suffering from bipolar depression.
The first drug, ketamine, is an experimental antidepressant that early studies have shown may quickly reduce suicidal thoughts, but we are not sure how well it may work. Midazolam, the comparison drug, is not thought to reduce depression or suicidal thoughts.
Detailed Description
Patients currently taking psychiatric medications may continue them during the study. However, if a patient is taking a benzodiazepine (such as Ativan, Klonopin, or Xanax), they will be able to take up to 2mg per day of Lorazepam during the week before the infusion, but none will be permitted in the 24 hours pre-infusion. Also, Zolpidem (Ambien) will not be permitted in the 24 hours pre-infusion. If a person chooses to participate, their dose of benzodiazepine may need to be reduced so that they can do without it during the 24 hours pre-infusion.
Participants are randomly assigned to receive a single dose of Ketamine (0.5 mg/kg) or Midazolam (0.02 mg/kg), which is given slowly, in a vein, over about 40 minutes. The study is "double-blind," meaning patients and study staff will not know which medication is in the infusion.
If a patient does not respond to the first infusion, and s/he received Midazolam, then s/he will be offered the option of a second infusion, this time with Ketamine (0.5 mg/kg). After the infusion(s), participants will have weekly research interviews for 6 weeks to monitor response.
After post-infusion research measures are completed, all subjects will receive open clinical treatment. During open clinical treatment, medication will be changed for those patients who don't respond or whose response is transient.
Participation in this study requires a brief inpatient stay, at no cost, at the New York State Psychiatric Institute (NYSPI).
Eligible participants enrolled in this study will be offered medication management visits at no cost for a total of up to 6 months combining inpatient and outpatient treatment. At the end of the 6 months of treatment patients will be referred for ongoing care.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder, Major Depressive Episode, Suicidal Ideation
Keywords
Ketamine, Midazolam, Bipolar Disorder, Major Depressive Episode, Suicidal Ideation, Suicide, Depression, Treatment, Ketamine Treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
16 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ketamine
Arm Type
Experimental
Arm Description
0.5 mg/kg, I.V. (in the vein)
Arm Title
Midazolam
Arm Type
Active Comparator
Arm Description
0.02 mg/kg, I.V. (in the vein)
Intervention Type
Drug
Intervention Name(s)
Ketamine
Other Intervention Name(s)
Ketalar, Ketamine Hydrochloride Injection
Intervention Description
Single dose of 0.5 mg/kg of Ketamine given intravenously (in the vein) over 40 minutes
Intervention Type
Drug
Intervention Name(s)
Midazolam
Other Intervention Name(s)
Midazolam Injection
Intervention Description
Single dose of 0.02 mg/kg of Midazolam given intravenously (in the vein) over 40 minutes
Primary Outcome Measure Information:
Title
Change in Suicidal Ideation Measured With the Beck Scale for Suicidal Ideation
Description
Change in suicidal ideation in Bipolar Disorder during a Major Depressive Episode (MDE), with moderate to severe suicidal thoughts, from the pre-infusion baseline to 24 hours after the infusion of Ketamine (study drug) or Midazolam (active control).
Time Frame
At 24 hours post-Infusion
Secondary Outcome Measure Information:
Title
Change in Systolic Blood Pressure
Description
Blood pressure is measured in millimeters of mercury.
Time Frame
During study infusion
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA:
Bipolar depression with current major depressive episode (MDE). Participants may be psychiatric medication-free, or if on psychiatric medication, not responding adequately given current MDE with suicidal ideation.
Moderate to severe suicidal ideation
18-65 years old
Patients will only be enrolled if they agree to voluntary admission to an inpatient research unit at the New York State Psychiatric Institute (NYSPI) for infusion phase of treatment.
Pre-menopausal female participants of child-bearing potential must be willing to use an acceptable form of birth control during study participation such as condoms, diaphragm, oral contraceptive pills
Able to provide informed consent
Subjects 61-65 years old must score 25 or higher on the Mini-Mental State Examination (MMSE) at screening
EXCLUSION CRITERIA:
Unstable medical condition or neurological illness, including baseline hypertension (BP>140/90) or significant history of cardiovascular illness
Significant ECG abnormality
Pregnancy and/or lactation
Current psychotic symptoms
Contraindication to any study treatment
Current or past ketamine abuse or dependence ever (lifetime); any other drug or alcohol dependence within past 6 months; suicidality only due to binge substance use or withdrawal
Inadequate understanding of English
Prior ineffective trial of or adverse reaction to ketamine or midazolam
Opiate use greater than total daily dose of 20mg Oxycodone or equivalent during the 3 days pre-infusion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael F Grunebaum, M.D.
Organizational Affiliation
Columbia Unviversity/New York State Psychiatric Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University/New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
12. IPD Sharing Statement
Links:
URL
http://www.columbiapsychiatry.org/mind/
Description
MIND Clinic for Mood and Personality Disorders
URL
http://abclocal.go.com/wabc/story?section=news/health&id=8975642
Description
Channel 7 NYC Story about Ketamine Research at Columbia University Medical Center
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Ketamine for Suicidality in Bipolar Depression
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