Liraglutide in Obesity and Diabetes: Identification of CNS Targets Using fMRI

PHASE4CompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

May 31, 2014

Study Completion Date

May 31, 2014

Conditions
DiabetesEffects of Liraglutide Administration on Brain ActivityWeight LossHunger
Interventions
DRUG

Liraglutide

In the experimental arm of this randomized, placebo controlled, cross-over, double-blinded study to assess the effects of liraglutide. Subjects will self-inject Liraglutide once per day for 18 days. Subjects will start the treatment with a dose of 0.6 mg for the first week, then 1.2 mg for the second week and 1.8 mg for 3 days in the third week.

DRUG

Placebo

In the placebo arm of this randomized, placebo controlled, cross-over, double-blinded study to assess the effects of liraglutide. Subjects will self-inject placebo once per day for 18 days.

Trial Locations (1)

02215

Beth Israel Deaconess Medical Center, Boston

All Listed Sponsors
lead

Beth Israel Deaconess Medical Center

OTHER

NCT01562678 - Liraglutide in Obesity and Diabetes: Identification of CNS Targets Using fMRI | Biotech Hunter | Biotech Hunter