The study will consist of a 24-week-long trial examining outcomes in patients with Major Depressive Disorder and suicidal ideation who will receive intravenous (IV) ketamine and intranasal (IN) esketamine, compared to a large sample of matched historical controls. Patients will be recruited from an inpatient psychiatric unit. Eligible patients who provided informed consent will be enrolled in the study that will include a eight IV ketamine treatments, 13 esketamine treatment visits, seven long assessment visits, five short assessment visits, and daily surveys. The study will examine the feasibility, tolerability, and efficacy of repeated IV ketamine followed by esketamine, as well as predictors of treatment response.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Study participants will start treatment including two ketamine infusion visits per week during the acute phase, for up to eight ketamine infusion visits. Participants will then be transitioned to maintenance with intranasal esketamine.
After one month from the eighth ketamine infusion visit, participants will initiate weekly esketamine for 12 weeks, for a total of 13 esketamine treatments. The esketamine visits will happen as per standard of care at the clinic and as instructed by the SPRAVATO Risk Evaluation and Mitigation Strategy.
Massachusetts General Hospital
Boston, Massachusetts, United States
RECRUITINGFeasibility - Retention
For examining the feasibility of treatment with ketamine and esketamine, descriptive analyses will be conducted to assess participants' retention across study visits.
Time frame: 24 weeks
Feasibility - Drop-out Rates
For examining the feasibility of treatment with ketamine and esketamine, descriptive analyses will be conducted to assess participants' drop-out rates across participation in the study.
Time frame: 24 weeks
Tolerability - Cognitive Function and Side Effects
In regard to tolerability, the investigators will closely monitor cognitive functions and side effects during the administration of ketamine and esketamine.
Time frame: Weeks 0, 1, 2, 3, 4, 8, and 12-24
Tolerability - Dosage of Treatment
In regard to tolerability, the investigators will record the Necessary Clinical Adjustments (NCAs) for dosage of ketamine and esketamine treatments.
Time frame: Change between weeks 0, 4, 6, 8, 10, 12, 14, 16, 20, 22, and 24
Tolerability - Frequency of Treatment
In regard to tolerability, the investigators will record the Necessary Clinical Adjustments (NCAs) for the frequency of ketamine and esketamine administration.
Time frame: Change between weeks 0, 4, 6, 8, 10, 12, 14, 16, 20, 22, and 24
Efficacy - Treatment Response
Descriptive analyses will be performed for percentage of responders (defined as 35% improvement on the QIDS-16) at the end of the IV ketamine acute phase, after the eighth ketamine infusion, and across the esketamine maintenance phase.
Time frame: Weeks 4, 8, and 12-24
Efficacy - Trajectory of Suicidal Ideation
The change in participants' suicidal ideation will be examined over time and compared to historical controls.
Time frame: 24 weeks
Efficacy - Trajectory of Depression
The change in participants' depression will be examined over time and compared to historical controls.
Time frame: 24 weeks
Efficacy - Hospital Readmission Rates
The change in participants' hospital readmission rates will be examined over time and compared to historical controls.
Time frame: 24 weeks
Efficacy - Prevalence of Suicidal Behavior
The occurrence of suicidal behavior (gestures, attempts, and completed suicide) among participants will be examined over time and compared to historical controls.
Time frame: 24 weeks
Efficacy - Healthcare Utilization
The change in participants' healthcare utilization rates will be examined over time and compared to historical controls.
Time frame: 24 weeks
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