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).
Ketamine for Suicidality in Bipolar Depression
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.
Intervention / Treatment
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Ketamine (DRUG)Single dose of 0.5 mg/kg of Ketamine given intravenously (in the vein) over 40 minutes
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Midazolam (DRUG)Single dose of 0.02 mg/kg of Midazolam given intravenously (in the vein) over 40 minutes
Condition or Disease
- Bipolar Disorder
- Major Depressive Episode
- Suicidal Ideation
Phase
Study Design
| Study type: | INTERVENTIONAL |
|---|---|
| Status: | Completed |
| Study results: | No Results Available |
| Age: | 18 Years to 65 Years |
| Enrollment: | 16 (ACTUAL) |
| Funded by: | Other |
| Allocation: | Randomized |
| Primary Purpose: | Treatment |
MaskingQUADRUPLE:
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Clinical Trial Dates
| Start date: | Sep 01, 2013 | |
|---|---|---|
| Primary Completion: | Sep 01, 2017 | ACTUAL |
| Completion Date: | Oct 01, 2018 | ACTUAL |
| Study First Posted: | Sep 17, 2013 | ESTIMATED |
| Results First Posted: | Jun 06, 2019 | ACTUAL |
| Last Updated: | Feb 27, 2020 |
Sponsors / Collaborators
Lead Sponsor:
New York State Psychiatric Institute
Responsible Party:
N/A
Location
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.
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.
Participant Groups
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0.5 mg/kg, I.V. (in the vein)
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0.02 mg/kg, I.V. (in the vein)
Eligibility Criteria
| Sex: | All |
|---|---|
| Minimum Age: | 18 |
| Maximum Age: | 65 |
| Age Groups: | Adult / Older Adult |
| Healthy Volunteers: | Yes |
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
* 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
Primary Outcomes
Secondary Outcomes
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Blood pressure is measured in millimeters of mercury.
More Details
| NCT Number: | NCT01944293 |
|---|---|
| Other IDs: | #6785 |
| Study URL: | https://clinicaltrials.gov/study/NCT01944293 |
Last updated: Sep 29, 2023