An Open Prospective Trial of IV Ketamine in Suicidal Adolescents

Status unconfirmed · Phase 2/Phase 3

Conditions studied: Major Depressive Disorder

In brief

1. 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. 2. 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.

Key facts

Study ID

NCT02048423

Run by

Nationwide Children's Hospital

People needed

10

Starts

2013-06-01

Expected to finish

2015-06-01

Last updated by the study team

2014-01-29

Who can join

Age: 12 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Nationwide Children's Hospital — Columbus, Ohio, United States (enrolling)

Full record on ClinicalTrials.gov

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