crossover randomized trial
S003172
Other conditionsS003172
Design
Conduct and analysis
Arms
| Arm | Treatment | Background | Randomized | Analyzed | Completed treatment |
|---|---|---|---|---|---|
| A1 | exenatide Exenatide IV infusion | lifestyle: not reported | 86 | 74 | |
| A2 | Placebo Placebo IV infusion | lifestyle: not reported | 86 | 74 | |
| A3 | Moxifloxacin Moxifloxacin 400 mg oral | lifestyle: not reported | 86 | 74 |
Baseline characteristics
As printed in the trial reports or registry, per arm or for the whole trial.
| Characteristic | Statistic | Exenatide IV infusion A1 | Placebo A2 | Moxifloxacin A3 | Whole trial ALL |
|---|---|---|---|---|---|
| age | mean (years) | 42 | |||
| age | sd (years) | 12 | |||
| bmi | mean (kg/m2) | 28.4 | |||
| bmi | sd (kg/m2) | 2.3 | |||
| other male | percent | 91 | |||
| white | percent | 73 |
Results
6 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
Serious adverse events (3 lines; O25)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| A1 | events | 0 / 86 | not stated; safety; R0026444:Results | ||||
| A2 | events | 0 / 86 | not stated; safety; R0026444:Results | ||||
| A3 | events | 0 / 86 | not stated; safety; R0026444:Results |
Death by suicide (3 lines; O35B)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| A1 | events | 0 / 86 | not stated; safety; R0026444:Results | ||||
| A2 | events | 0 / 86 | not stated; safety; R0026444:Results | ||||
| A3 | events | 0 / 86 | not stated; safety; R0026444:Results |