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Spravato (Esketamine) in Hartford, Connecticut

Compare 2 Spravato (Esketamine) clinics in Hartford, Connecticut that offer care for treatment-resistant depression and major depressive disorder. Review services, ratings, and contact details to find the right provider near you.
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Clinics

2 clinics shown

  • Center Building - Institute of Living

    The Institute of Living operates a psychiatric hospital on Retreat Avenue in Hartford, providing inpatient and outpatient mental health services for adults and adolescents. The facility treats mood disorders, psychotic disorders, substance use disorders, and trauma-related conditions through multidisciplinary care teams. Specific procedural treatments such as TMS or esketamine are not detailed in available information; prospective patients should contact the hospital directly to confirm current treatment modalities and admission criteria.

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  • State of Connecticut Department of Mental Health and Addiction Services

    The Connecticut Department of Mental Health and Addiction Services operates a state facility on Capitol Avenue in Hartford, providing public mental health and substance use disorder services to residents across the state system. This administrative and clinical location coordinates care for individuals requiring state-funded psychiatric treatment, crisis intervention, and addiction services. Specific treatment modalities such as TMS or esketamine are not detailed in available information; patients should contact the department directly to determine which evidence-based treatments are offered at this location versus other DMHAS facilities statewide.

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About Spravato (Esketamine)

Spravato is the brand name for esketamine, an FDA-approved nasal spray for treatment-resistant depression and major depressive disorder with suicidal ideation. It's derived from ketamine and works on the brain's glutamate system — a different mechanism than traditional antidepressants like SSRIs.

Treatment is administered only at REMS-certified clinics under direct medical supervision. Patients self-administer the spray under a clinician's guidance, then remain at the clinic for at least two hours of monitoring after each dose. The induction phase typically involves twice-weekly sessions for four weeks, followed by weekly or biweekly maintenance dosing depending on response.

Many patients report meaningful symptom improvement within the first one to two weeks — substantially faster than the 4 to 8 weeks typical of oral antidepressants. Spravato is taken alongside an oral antidepressant, not as a replacement.

The most common side effects are dissociation, dizziness, sedation, and elevated blood pressure during and shortly after dosing. These typically resolve within the two-hour monitoring window. Patients cannot drive on the day of treatment.

Most commercial insurance and Medicare cover Spravato for treatment-resistant depression with prior authorization. Clinics offering Spravato in our directory hold active REMS certification and are staffed to provide the required in-clinic monitoring period.