Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
Location status: Recruiting
Location contact
Catherine Schuessler, BS
CONTACT
Catherine Schuessler, BS
CONTACT
Cristina Cusin, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT05450432
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.
Interested in participating?
Request Info18 year–70 year
All sexes
Interventional
Phase 4
Boston, Massachusetts, 02114, United States
Location status: Recruiting
Catherine Schuessler, BS
CONTACT
Catherine Schuessler, BS
CONTACT
Cristina Cusin, MD
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
g. Patients with a history of narrow angle glaucoma - untreated 14. Inability to comply with ketamine clinic safety procedures, including having reliable escorts to and from visits.
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.
Time frame: 24 weeks
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
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: Weeks 0, 1, 2, 3, 4, 8, and 12-24
In regard to tolerability, the investigators will closely monitor cognitive functions and side effects during the administration of ketamine and esketamine.
Time frame: Change between weeks 0, 4, 6, 8, 10, 12, 14, 16, 20, 22, and 24
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
In regard to tolerability, the investigators will record the Necessary Clinical Adjustments (NCAs) for the frequency of ketamine and esketamine administration.
Time frame: Weeks 4, 8, and 12-24
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: 24 weeks
The change in participants' suicidal ideation will be examined over time and compared to historical controls.
Time frame: 24 weeks
The change in participants' depression will be examined over time and compared to historical controls.
Time frame: 24 weeks
The change in participants' hospital readmission rates will be examined over time and compared to historical controls.
Time frame: 24 weeks
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
The change in participants' healthcare utilization rates will be examined over time and compared to historical controls.
Time frame: 24 weeks
Exploratory aims will be examined, including predictors of treatment response (defined as 35% improvement in QIDS score) at the end of the acute and maintenance phases.
Time frame: 24 weeks
Exploratory aims will be examined, including predictors of suicidal ideation relapse (defined as SSI5>1) during time intervals between intravenous ketamine visits and during the esketamine maintenance phase.
Contact information is provided by the study sponsor or research team.
Catherine Schuessler, BS
CONTACT
Cristina Cusin, MD
CONTACT
Massachusetts General Hospital
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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