parallel randomized trial
S002963
Other conditionsS002963
Design
Conduct and analysis
Arms
| Arm | Treatment | Background | Randomized | Analyzed | Completed treatment |
|---|---|---|---|---|---|
| A1 | Liraglutide 3.0 mg subcutaneous once daily Liraglutide 3.0 mg plus escitalopram | escitalopram 20 mg once daily; lifestyle: not reported | |||
| A2 | Placebo 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.
| Characteristic | Statistic | Liraglutide 3.0 mg subcutaneous once daily A1 | Placebo A2 | Whole trial ALL |
|---|---|---|---|---|
| age | mean (years) | 41.2 | ||
| bmi | mean (kg/m2) | 33.9 | ||
| female | percent | 60 |