Journal of Psychopharmacology
March 1, 2020
P. Glue, Shona Neehoff, A. Sabadel et al.
97 citations
In a double-blind, psychoactive-controlled study, 12 patients with treatment-resistant generalized anxiety and social anxiety disorders who were not currently depressed received ascending doses of ketamine (0.25, 0.5, 1 mg/kg) at weekly intervals, with midazolam 0.01 mg/kg randomly inserted as a control. Improvements in anxiety ratings occurred within an hour of ketamine dosing and persisted for up to one week. A dose-response profile was noted for anxiolytic effects, dissociative side effects, and changes in blood pressure and heart rate. Midazolam had minor brief effects on anxiety ratings. Ketamine was safe and well tolerated. Ketamine may be a potential therapeutic option for these patients.
BJPsych Open
October 1, 2025
Ben Beaglehole, Paul Glue, Shona Neehoff et al.
5 citations
Intramuscular ketamine shows preliminary effectiveness and is well tolerated by people with posttraumatic stress disorder in a community setting. The findings are encouraging given the known limitations of existing treatments, but more research is needed to determine the best dosing schedule and long-term role of ketamine for PTSD.
The International Journal of Neuropsychopharmacology
July 6, 2026
Shabah M. Shadli, Neda Nasrollahi, Calvin K. Young et al.
Ketamine at low doses (0.5-1.0 mg/kg I.M.) quickly reduces symptoms in treatment-resistant major depressive disorder (TR-MDD), post-traumatic stress disorder (TR-PTSD), and obsessive-compulsive disorder (TR-OCD), but its neural effects differ by diagnosis. EEG recordings of resting frontal activity before and after ketamine or fentanyl showed that TR-PTSD patients had dose- and band-frequency-dependent power changes (especially alpha at 0.5 mg/kg), while TR-MDD patients showed no such changes. TR-OCD responses differed qualitatively from both. Correlations between EEG power changes and symptom scale improvements varied by band and electrode across different disorder-specific scales. Ketamine's effects and their therapeutic links vary by brain site and frequency band depending on the DSM diagnosis, suggesting disorder-specific systems require a ketamine-sensitive factor to generate the disorder.