A structured, medically supervised treatment for individuals who have not improved with traditional options
Spravato® is an FDA‑approved treatment used when traditional antidepressants have not provided enough improvement. It is administered in‑office under medical supervision, with time dedicated to monitoring, discussion, and clinical evaluation throughout the visit.
Spravato® may be considered when symptoms remain despite multiple treatment attempts.
A session begins with a brief check‑in and review of recent changes. The medication is self‑administered under supervision, followed by a quiet monitoring period. There is space to discuss how the treatment feels, any side effects, and what has changed since the previous visit. The visit ends once clinical criteria for discharge are met.
Spravato® offers a structured approach for individuals who have not improved with standard treatments.
Spravato® works through NMDA‑receptor modulation, offering an alternative pathway for individuals who have not improved with traditional antidepressants. Treatment is administered in‑office as a supervised nasal spray, followed by a quiet monitoring period and a structured clinical review. Each visit lasts about two hours, with dosing frequency adjusted over time based on response and tolerability.
Spravato® follows a structured schedule that adjusts over time based on response and tolerability.
Week 1–4
Two treatments per week
Week 5–8
One treatment
per week
Week 9
Maintenance dosing as needed
Week 9
Maintenance dosing as needed
Most visits last around two hours, including monitoring time.
No. It must be administered in‑office under supervision.
Experiences vary. Some individuals notice shifts within the first few weeks.
No. It is optional and used when medication precision may be helpful.
Yes. It is often used alongside ongoing therapy or medication management.
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