Intranasal Ketamine for Suicidal Ideation in Veterans

To address the significant need for effective treatment of suicidal ideation in Veterans,
this trial is designed as an open label pilot study of intranasal ketamine in 15 people.

Inclusion Criteria:

1. Male or female patients, 21-70 years of age

2. Female individuals who are not of childbearing potential (i.e., surgically sterile,
postmenopausal for at least one year) or using a medically accepted reliable means of
contraception. Women using oral contraceptive medication for birth control must also
be using a barrier contraceptive. Women of childbearing potential must also have a
negative pregnancy test at screening and at pre-administration

3. Any non-psychotic disorder diagnosis

4. Score >4 on the suicide item of the Montgomery-Asberg Depression Rating Scale
(MADRS-SI; range 0-6)for clinically significant suicidal ideation or past suicide
attempts

5. Each participant must have a level of understanding sufficient to agree to all tests
and examinations required by the protocol and must sign an informed consent document

6. Each participant must agree to avoid future enrollment in ketamine trials.

Exclusion Criteria:

1. current psychotic symptoms or lifetime history of primary psychotic disorder

2. active substance use in the preceding two weeks or needing medical attention for
withdrawal

3. neurodevelopmental disorder (e.g., ASD)

4. major neurocognitive disorder (e.g., Alzheimer's type dementia)

5. serious cardiac disease

6. suicide attempt precipitating current admission requiring medical stabilization

7. Lifetime histories of autism, mental retardation, pervasive developmental disorders,
or Tourette's syndrome

8. Women who are either pregnant or nursing

9. Hypertension (systolic BP >160 mm Hg or diastolic BP >90 mm Hg) at screening or
immediately prior to treatment with study drug

10. Previously received ketamine for refractory depression.