Repeated Ketamine Infusions for Comorbid PTSD and MDD in Veterans
Post-Traumatic Stress Disorders, Major Depressive Disorder
About this trial
This is an interventional diagnostic trial for Post-Traumatic Stress Disorders focused on measuring ketamine, stress disorders, post-traumatic, stress disorders, traumatic, anxiety disorders, mental disorders, adjuvants, anesthesia, analgesics, anesthetics, anesthetics, dissociative, anesthetics, general, anesthetics, intravenous, excitatory amino acid agents, excitatory amino acid antagonists, hypnotics and sedatives, molecular mechanisms of pharmacological action, neurotransmitter agents, peripheral nervous system agents, pharmacologic actions, physiological effects of drugs, psychotropic drugs, sensory system agents, central nervous system agents, central nervous system depressants, depression, depressive disorder, depressive disorder, treatment-resistant, behavioral symptoms, mood disorders, therapeutic uses
Eligibility Criteria
Inclusion Criteria:
For the PTSD+MDD group, inclusion criteria are:
- Female/Male veterans
- 18 to 75 years old
- Meets DSM-5 criteria for MDD, single or recurrent, moderate-severe without psychotic features
- Meets DSM-5 criteria for chronic PTSD or subthreshold PTSD [meets criterion A (traumatic event), criterion B (intrusion symptoms), and 2 of the following 3 criteria: C (avoidance symptoms), D (negative alterations in cognitions and mood), or E (marked alterations in arousal and reactivity)]
- If applicable, 6 weeks of stable antidepressants/augmenting agents
- Sixth grade reading level
- Ability to provide consent
For the Healthy Controls group, inclusion criteria are:
- Female/Male veterans
- 18 to 75 years old
- Does not meet DSM-5 criteria for MDD, single or recurrent, moderate-severe without psychotic features
- Does not meet DSM-5 criteria for chronic PTSD or subthreshold PTSD
- Not on medications for managing a psychiatric indication
- Sixth grade reading level
- Ability to provide consent
For the Depression-only group, inclusion criteria are:
- Female/Male veterans
- 18 to 75 years old
- Experienced a traumatic event that meets DSM-5 criterion A for a diagnosis of PTSD but does not meet sufficient criteria (B-E) necessary for a diagnosis of PTSD or subthreshold PTSD
- Meets criteria for MDD, single or recurrent, moderate-severe
- If applicable, 6 weeks of stable antidepressants/augmenting agents
- Sixth grade reading level
- Ability to provide consent
For the PTSD-only group, inclusion criteria are:
- Female/Male veterans
- 18 to 75 years old
- Meets DSM-5 criteria for chronic PTSD or subthreshold PTSD [meets criterion A (traumatic event), criterion B (intrusion symptoms), and 2 of the following 3 criteria: C (avoidance symptoms), D (negative alterations in cognitions and mood), or E (marked alterations in arousal and reactivity)]
- Does not meet DSM-5 criteria for MDD, single or recurrent, moderate-severe without psychotic features
- If applicable, 6 weeks of stable antidepressants/augmenting agents
- Sixth grade reading level
- Ability to provide consent
Exclusion Criteria:
For the PTSD+MDD group, exclusion criteria are:
- Inability or unwillingness to provide written informed consent
- Moderate/severe cognitive impairment
- Current or lifetime diagnosis of psychosis-related disorder, bipolar I or II disorder, substance-induced mood disorder, or any mood disorder due to a general medical condition
- History of moderate or severe traumatic brain injury
- History of comorbid substance disorder within 1 month of screening
- Prior use of ketamine as an antidepressant
- Clinically unstable medical illness
- For women: pregnancy (confirmed by baseline lab test), the initiation of female hormonal treatments within 3 months of screening, or inability or unwillingness to use a medically accepted contraceptive method for the duration of the study
- Imminent risk of suicidal/homicidal ideation and/or behavior
- Inability to undergo MRI (i.e. claustrophobia, ferromagnetic implants, etc.)
For the Healthy Controls group, exclusion criteria are:
- Inability or unwillingness to provide written informed consent
- Moderate/severe cognitive impairment
- History of any major medical or psychiatric disorders
- Current or lifetime diagnosis of psychosis-related disorder, bipolar I or II disorder, substance-induced mood disorder, or any mood disorder due to a general medical condition
- History of moderate or severe traumatic brain injury
- History of comorbid substance disorder within 1 month of screening
- Prior use of ketamine as an antidepressant
- Clinically unstable medical illness
- For women: pregnancy (confirmed by baseline lab test), the initiation of female hormonal treatments within 3 months of screening, or inability or unwillingness to use a medically accepted contraceptive method for the duration of the study
- Imminent risk of suicidal/homicidal ideation and/or behavior
- Inability to undergo MRI (i.e. claustrophobia, ferromagnetic implants, etc.)
For the Depression-only group, exclusion criteria are:
- Inability or unwillingness to provide written informed consent
- Moderate/severe cognitive impairment
- Meet DSM-5 criteria for PTSD or subthreshold PTSD
- Current or lifetime diagnosis of psychosis-related disorder, bipolar I or II disorder, substance-induced mood disorder, or any mood disorder due to a general medical condition
- History of moderate or severe traumatic brain injury
- History of comorbid substance disorder within 1 month of screening
- Prior use of ketamine as an antidepressant
- Clinically unstable medical illness
- For women: pregnancy (confirmed by baseline lab test), the initiation of female hormonal treatments within 3 months of screening, or inability or unwillingness to use a medically accepted contraceptive method for the duration of the study
- Imminent risk of suicidal/homicidal ideation and/or behavior
- Inability to undergo MRI (i.e. claustrophobia, ferromagnetic implants, etc.)
For the PTSD-only group, exclusion criteria are:
- Inability or unwillingness to provide written informed consent
- Moderate/severe cognitive impairment
- Meet DSM-5 criteria for a diagnosis of MDD, single or recurrent, moderate to severe
- Current or lifetime diagnosis of psychosis-related disorder, bipolar I or II disorder, substance-induced mood disorder, or any mood disorder due to a general medical condition
- History of moderate or severe traumatic brain injury
- History of comorbid substance disorder within 1 month of screening
- Prior use of ketamine as an antidepressant
- Clinically unstable medical illness
- For women: pregnancy (confirmed by baseline lab test), the initiation of female hormonal treatments within 3 months of screening, or inability or unwillingness to use a medically accepted contraceptive method for the duration of the study
- Imminent risk of suicidal/homicidal ideation and/or behavior
- Inability to undergo MRI (i.e. claustrophobia, ferromagnetic implants, etc.)
Sites / Locations
- Minneapolis Veterans Affairs Health Care SystemRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Intravenous ketamine infusions
Intravenous saline infusions
Six infusions of 0.5 mg/kg ketamine hydrochloride solution over 3 weeks.
Six infusions of normal saline solution over 3 weeks.