parallel randomized trial
S003034
Other conditionsS003034
Design
Conduct and analysis
Arms
| Arm | Treatment | Background | Randomized | Analyzed | Completed treatment |
|---|---|---|---|---|---|
| A1 | Liraglutide 1.8 mg subcutaneous once daily Liraglutide 1.8 mg daily | lifestyle: not reported | 26 | ||
| A2 | Colesevelam Colesevelam 1875 mg twice daily | lifestyle: not reported | 26 |
Baseline characteristics
As printed in the trial reports or registry, per arm or for the whole trial.
| Characteristic | Statistic | Liraglutide 1.8 mg subcutaneous once daily A1 | Colesevelam A2 | Whole trial ALL |
|---|---|---|---|---|
| age | mean (years) | 51.7 | 48.7 | |
| age | sd (years) | 13.3 | 12.8 | |
| bmi | mean (kg/m2) | 31.5 | 28.3 | |
| bmi | sd (kg/m2) | 5.6 | 4.1 | |
| female | n | 32 |
Results
4 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
Discontinuation due to adverse events (2 lines; O26)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| A1 | events | 1 / 26 | not stated; randomized; R0018327:Results | ||||
| A2 | events | 1 / 26 | not stated; randomized; R0018327:Results |
Discontinuation due to gastrointestinal adverse events (2 lines; O27E)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| A1 | events | 1 / 26 | not stated; randomized; R0018327:Results | ||||
| A2 | events | 1 / 26 | not stated; randomized; R0018327:Results |