Advancing Personalized Antidepressant Treatment Using PET/MRI

PHASE4CompletedINTERVENTIONAL
Enrollment

85

Participants

Timeline

Start Date

May 31, 2015

Primary Completion Date

March 31, 2020

Study Completion Date

March 31, 2020

Conditions
Depression
Interventions
DRUG

Escitalopram

Participants randomized to the escitalopram group will be given the medication for 8 weeks, after which they will be given the option to continue for 4 more weeks if they are close to remission. This additional 4-week treatment option is something offered to participants outside the clinical trial, and therefore was not treated as part of the main study.

DRUG

Placebo

To reduce the burden of the patients on placebo, the placebo trial will have a target of 8 weeks. To provide an opportunity for placebo non-responders to receive active drug and to aid in recruitment, we will provide 8-12 weeks of SSRI treatment to placebo non-responders. This treatment option is something offered to participants outside the clinical trial, and therefore was not treated as part of the main study.

Trial Locations (1)

11794

Stony Brook University Hospital, Stony Brook

All Listed Sponsors
lead

Stony Brook University

OTHER

NCT02623205 - Advancing Personalized Antidepressant Treatment Using PET/MRI | Biotech Hunter | Biotech Hunter