An Open Prospective Trial of IV Ketamine in Suicidal Adolescents
Primary Purpose
Major Depressive Disorder
Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Ketamine
Sponsored by
About this trial
This is an interventional treatment trial for Major Depressive Disorder focused on measuring suicidal
Eligibility Criteria
Inclusion Criteria
- Subjects age 12 years 0 months to 17 years, 11 months old
- Voluntary admission for a suicide attempt requiring medical intervention in the previous 24-48 hours (Kiddie Schedule for Affective Disorders Suicide Behavior Score > 3).
- Meets criteria for major depression, single- or recurrent episode, non-psychotic or Bipolar I, current episode depressed, with a baseline Inventory for depression score of > 16.
- The patient and legal guardian must understand the nature of the study and be able to comply with protocol requirements. The legal guardian must give written informed consent and the youth, written assent.
- English is spoken as the primary language in the home.
Exclusion Criteria
- Any serious, unstable medical illness or clinically significant abnormal laboratory assessments that would adversely impact the scientific interpretability or unduly increase the risks of the protocol.
- Admitted to Nationwide Children's Hospital involuntarily.
- Unable to assent because of severe mental retardation or incapacitating psychosis.
- Other medications: See Table 1. The list in Table 1 is not exhaustive. The Principal Investigator and the Co-Investigator will review all concomitant medicines and any medicine that could interfere with the trial will be considered exclusionary. Subjects with bipolar disorder will be allowed to continue their mood stabilizers and or antipsychotic agents at the discretion of the investigator. Stimulants use is acceptable, though the child must be on a stable dose for the past 3 months and the dose must not be changed through the trial. A stable dose is defined as no more that 25% change in the total daily dose of a stimulant.
- General medical conditions: children with major medical conditions that would interfere with involvement in the study or the study medication will not be enrolled.
- Exclusionary Psychiatric Conditions: Autism, substance dependence, psychosis or psychotic major depression.
- History of physical, sexual, or emotional abuse, which results in a clinically significant impact on clinical presentation, potentially driving some of the symptoms of major depressive disorder.
- Receipt of an investigational drug within 30 days prior to study entry.
Sites / Locations
- Nationwide Children's HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Ketamine
Arm Description
Drug
Outcomes
Primary Outcome Measures
Change in Quick Inventory of Depression Clinician (QIDS-C) total scores from baseline to endpoint and Clinical Global Improvement Score.
Secondary Outcome Measures
Clinical Global Assessment Scale
Full Information
NCT ID
NCT02048423
First Posted
August 2, 2013
Last Updated
January 27, 2014
Sponsor
Nationwide Children's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02048423
Brief Title
An Open Prospective Trial of IV Ketamine in Suicidal Adolescents
Official Title
An Open Prospective Trial of IV Ketamine in Suicidal Adolescents
Study Type
Interventional
2. Study Status
Record Verification Date
January 2014
Overall Recruitment Status
Unknown status
Study Start Date
June 2013 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
June 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nationwide Children's Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Investigate the safety and effectiveness of a single dose of IV Ketamine for adolescents with suicidal ideation and depression. It is hypothesize that Ketamine will be well tolerated and significantly reduce depressive symptoms and suicidal ideation.
Explore whether decision making as measured by the Iowa Gambling Task changes before and after Ketamine infusion. It is hypothesize that IV Ketamine infusion will significantly improve the decision making ability a measured by the Iowa Gambling Task in adolescents that are suicidal.
Detailed Description
This is an open prospective study of a single, low dose (0.5 mg/kg) intravenous (IV) Ketamine in 10 adolescent subjects admitted to Nationwide Childrens Hospital following a serious suicide attempt and who meet criteria for major depression or bipolar disorder I, current episode depressed. Subjects will be recruited via the psychiatry consult service, evaluated on the floor and if eligible and consent is obtained, transferred to the PACU for IV Ketamine infusion. Following infusion and when PACU discharge criteria are met, subjects will be transferred back to their floor for medical and psychiatric monitoring until they can be transferred to an inpatient psychiatric unit for additional care. Subjects will be transferred to an inpatient psychiatric unit for continued psychiatric care as part of their routine psychiatric care via the consult team. The research team will follow-up by telephone one week and four weeks after Ketamine injection to collect additional information about the patient's overall course and response.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder
Keywords
suicidal
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Ketamine
Arm Type
Experimental
Arm Description
Drug
Intervention Type
Drug
Intervention Name(s)
Ketamine
Other Intervention Name(s)
Ketaset, Ketalean, Rogarsetic
Intervention Description
IV Ketamine, 0.5 mg/kg X 15 mins. in PACU
Primary Outcome Measure Information:
Title
Change in Quick Inventory of Depression Clinician (QIDS-C) total scores from baseline to endpoint and Clinical Global Improvement Score.
Time Frame
2 days
Secondary Outcome Measure Information:
Title
Clinical Global Assessment Scale
Time Frame
2 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
Subjects age 12 years 0 months to 17 years, 11 months old
Voluntary admission for a suicide attempt requiring medical intervention in the previous 24-48 hours (Kiddie Schedule for Affective Disorders Suicide Behavior Score > 3).
Meets criteria for major depression, single- or recurrent episode, non-psychotic or Bipolar I, current episode depressed, with a baseline Inventory for depression score of > 16.
The patient and legal guardian must understand the nature of the study and be able to comply with protocol requirements. The legal guardian must give written informed consent and the youth, written assent.
English is spoken as the primary language in the home.
Exclusion Criteria
Any serious, unstable medical illness or clinically significant abnormal laboratory assessments that would adversely impact the scientific interpretability or unduly increase the risks of the protocol.
Admitted to Nationwide Children's Hospital involuntarily.
Unable to assent because of severe mental retardation or incapacitating psychosis.
Other medications: See Table 1. The list in Table 1 is not exhaustive. The Principal Investigator and the Co-Investigator will review all concomitant medicines and any medicine that could interfere with the trial will be considered exclusionary. Subjects with bipolar disorder will be allowed to continue their mood stabilizers and or antipsychotic agents at the discretion of the investigator. Stimulants use is acceptable, though the child must be on a stable dose for the past 3 months and the dose must not be changed through the trial. A stable dose is defined as no more that 25% change in the total daily dose of a stimulant.
General medical conditions: children with major medical conditions that would interfere with involvement in the study or the study medication will not be enrolled.
Exclusionary Psychiatric Conditions: Autism, substance dependence, psychosis or psychotic major depression.
History of physical, sexual, or emotional abuse, which results in a clinically significant impact on clinical presentation, potentially driving some of the symptoms of major depressive disorder.
Receipt of an investigational drug within 30 days prior to study entry.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Robert A Kowatch, MD, PhD
Phone
614-355-2872
Email
robert.kowatch@nationwidechildrens.org
First Name & Middle Initial & Last Name or Official Title & Degree
Melinda Helton, Pharm
Phone
614-722-2607
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert A Kowatch, MD, PhD
Organizational Affiliation
OSU Medical Center/Nationwide Childrens Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nationwide Children's Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Melinda Helton, RN
Phone
614-722-2607
12. IPD Sharing Statement
Learn more about this trial
An Open Prospective Trial of IV Ketamine in Suicidal Adolescents
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