The Honest State of the Evidence
Rodriguez and colleagues ran a randomized crossover trial in unmedicated OCD patients and reported rapid reduction in obsessive symptoms after a single ketamine infusion. It is a real result and worth taking seriously. It is also a small proof-of-concept study, and the replication literature has not caught up with it. Treating that as equivalent to the depression evidence would misrepresent where things stand.
- A single small randomized crossover trial, not a body of replicated work
- The studied population was unmedicated, unlike most patients who contact us
- Effect on obsessions was clearer than effect on compulsions
- Durability beyond the short term is not well characterized
- Depression research does not transfer automatically to OCD
ERP Comes First, and That Is Not a Formality
Exposure and response prevention has the strongest outcome evidence of any OCD treatment, medication included. If you have not had a proper ERP course with a therapist trained in it, that is the highest-value next step and it is not close. A large share of people who believe ERP failed them actually had supportive talk therapy about their OCD, which is a different thing and does not work for OCD.
- ERP has the strongest evidence base in OCD, ahead of medication
- Generic talk therapy about obsessions is not ERP and often makes OCD worse
- Reassurance-seeking within therapy can function as a compulsion
- High-dose SSRIs for OCD exceed typical depression dosing and take longer to judge
- Twelve weeks at an adequate OCD dose is the standard before calling an SSRI failed
What Ketamine Might Add
The mechanistic case rests on glutamate. OCD involves the cortico-striato-thalamo-cortical loop, and glutamatergic dysregulation within that circuit is a recurring finding. Ketamine acts directly on that system rather than on serotonin, which is a different lever from every first-line OCD medication. The plausible use is opening a window in which ERP is more tolerable for someone too symptomatic to engage with it.
- Direct glutamatergic action, unlike SSRIs which act on serotonin
- CSTC loop involvement is well described in OCD neuroimaging
- Possible role in making ERP tolerable for severely symptomatic patients
- Not a substitute for ERP and not positioned as one here
- Co-occurring depression is often the more evidence-supported target
Who Should Not Start Here
This page turns more people away than it accepts, deliberately. OCD is highly treatable with the right therapy, and starting with an off-label intervention that has one small trial behind it is usually the wrong order of operations.
- Anyone who has not had a genuine ERP course with a trained therapist
- Anyone who has not completed an adequate high-dose SSRI trial for OCD
- Patients whose primary distress is a related but distinct condition
- Anyone seeking certainty or reassurance, which ketamine cannot supply
- Active substance use disorder, psychosis, or untreated bipolar mania
If You Do Proceed
For patients who have done the first-line work and remain significantly impaired, particularly where depression sits alongside the OCD, a course here is reasonable. It runs as physician-led care with the same doctor throughout and booking windows that extend past the standard clinic day.
- Screening scored before consultation, including depression severity
- Video consultation with Dr. Ben Soffer, DO, and a full medication review
- Extended booking windows including 12:30 PM and 5:00 PM appointments
- Sublingual medication shipped to your home, with a sober support person required
- Continued ERP encouraged throughout, not paused for treatment
