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Ketamine and Internalizing Disorders

Ketamine Therapy For Internalizing Disorders: Is There A Single Mechanism?

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000311156
Acronym
KIDs
Enrollment
14
Registered
2019-02-28
Start date
2020-11-02
Completion date
2023-05-31
Last updated
2021-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Internalizing disorders, characterized by quiet, internal distress, include DSM5 diagnoses such as Generalized Anxiety Disorder, Social Anxiety Disorder, Major Depressive Disorder, Panic Disorder, Post-Traumatic Stress Disorder, Obsessive Compulsive Disorder and phobic states. In contrast to slow and variable responsiveness to conventional medications, ketamine is rapidly effective in all internalizing disorders assessed so far. To account for these differences in speed of onset and breadth of activity between conventional treatments and ketamine, we have recently proposed a ‘double hit’ model for internalizing disorders, with 2 distinct forms of neural dysfunction to coincide. One hit, which is sensitive to ketamine, is disorder general: dysfunction of a neural system linked to high levels of the personality trait of neuroticism. The other hit is disorder-specific: dysfunction of one of a set of disorder-specific neural modules (already identified by theory), each with its own particular pattern of sensitivity to conventional drugs. We predict that ketamine will produce similar right frontal EEG changes that will correlate with symptom improvement across all of these internalizing disorders. These findings will potentially provide clinicians and researchers with results that could produce major theoretical advances (e.g. for reclassification of anxiety and depressive disorders) and may support wider use of ketamine as a treatment for internalizing disorders.

Interventions

There are 4 groups; treatment-resistant MDE, OCD, PTSD, phobic states. Each participant will receive a single dose of each of these treatments plus a psychoactive control, with a washout of at least 7 days between treatments: Ketamine 0.5mg/kg intramuscular injection, single dose Ketamine 1mg/kg intramuscular injection, single dose

Sponsors

University of Otago
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

• Capable of understanding and signing an informed consent • diagnosed with one of the following DSM-5 diagnoses: -post-traumatic stress disorder (PTSD) with a CAPS score >60; -obsessive-compulsive disorder (OCD) with a YBOCS score >26; -major depressive disorder (MDD) with a MADRS score >20; -phobic state with FQ18 score >6 • Patients with PTSD, OCD or phobic state must not have MADRS scores >20 at screening. • Patients must have had an inadequate response to prior treatment i.e. have not responded to at least two adequate trials of relevant medication and at least one trial of relevant psychotherapy.

Exclusion criteria

• evidence of severe acute or chronic medical disorders, • past or current diagnoses of schizophrenia, bipolar disorder, or current psychotic symptoms • female patients who are pregnant or lactating • drug use or dependence in the last 6 months • current significant suicidal ideation • prior history of seizures; susceptibility to photosensitivity; or a history of allergic skin reactions

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026