LivingGLP1
parallel randomized trial

S002963

Design

Randomized
Start year
Treatment
6 weeks, follow-up 6 weeks
Countries
Sponsor
(not reported)
Eligibility
major depressive disorder, BMI 27 or more, HDRS above 20

Conduct and analysis

Blinding
double blind
Sequence generation
not reported
Allocation concealment
not reported
Outcome adjudication
not reported
Primary estimand
not stated
Analysis population
Missing data

Arms

ArmTreatmentBackgroundRandomizedAnalyzedCompleted treatment
A1Liraglutide 3.0 mg subcutaneous once daily
Liraglutide 3.0 mg plus escitalopram
escitalopram 20 mg once daily; lifestyle: not reported
A2Placebo
Placebo plus escitalopram
escitalopram 20 mg once daily; lifestyle: not reported

Baseline characteristics

As printed in the trial reports or registry, per arm or for the whole trial.
CharacteristicStatisticLiraglutide 3.0 mg subcutaneous once daily
A1
Placebo
A2
Whole trial
ALL
agemean (years)41.2
bmimean (kg/m2)33.9
femalepercent60