parallel randomized trial
S003426
Type 2 diabetes (adults)S003426
Design
Conduct and analysis
Arms
| Arm | Treatment | Background | Randomized | Analyzed | Completed treatment |
|---|---|---|---|---|---|
| A1 | Semaglutide 0.5 mg subcutaneous once weekly Semaglutide 0.5 mg once weekly | metformin 2 g/day and empagliflozin 25 mg/day; lifestyle: standard | 38 | 38 | |
| A2 | Tirzepatide 5 mg subcutaneous once weekly Tirzepatide 5 mg once weekly | metformin 2 g/day and empagliflozin 25 mg/day; lifestyle: standard | 41 | 41 |
Baseline characteristics
As printed in the trial reports or registry, per arm or for the whole trial.
| Characteristic | Statistic | Semaglutide 0.5 mg subcutaneous once weekly A1 | Tirzepatide 5 mg subcutaneous once weekly A2 |
|---|---|---|---|
| age sex:female | mean (years) | 47.0 | 48.0 |
| age sex:male | mean (years) | 52.0 | 50.5 |
| bmi | mean (kg/m2) | 33.8 | 34.2 |
| female | n | 22 | 27 |
| female | percent | 57.9 | 65.9 |
| hba1c | mean (percent) | 7.7 | 7.9 |
Analyses this trial contributes to
- Level 2 or 3 hypoglycemia (participants)Type 2 diabetes (adults); longest follow-up; network meta-analysis
- Level 2 or 3 hypoglycemia (participants)Type 2 diabetes (adults); longest follow-up; network meta-analysis
- Discontinuation due to adverse eventsType 2 diabetes (adults); longest follow-up; network meta-analysis
- Discontinuation due to adverse eventsType 2 diabetes (adults); longest follow-up; network meta-analysis
- Discontinuation due to gastrointestinal adverse eventsType 2 diabetes (adults); longest follow-up; network meta-analysis
- Discontinuation due to gastrointestinal adverse eventsType 2 diabetes (adults); longest follow-up; network meta-analysis
Results
11 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
HbA1c change (3 lines; O01)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| 24 | A1 | change | -0.9 percent | 38 | not stated; other; R0040396:Table 2 | ||
| 24 | A1 vs A2 | md | 0.5 percent | not stated; other; R0040396:Table 2 | |||
| 24 | A2 | change | -1.4 percent | 41 | not stated; other; R0040396:Table 2 |
Level 2 or 3 hypoglycemia (participants) (3 lines; O04)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| A1 | events | 1 / 38 | not stated; safety; R0040396:Table 3 | ||||
| A1 vs A2 | or | 0.53 | not stated; safety; R0040396:Table 3 | ||||
| A2 | events | 2 / 41 | not stated; safety; R0040396:Table 3 |
Discontinuation due to adverse events (2 lines; O26)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| A1 | events | 3 / 38 | not stated; safety; R0040396:Abstract | ||||
| A2 | events | 2 / 41 | not stated; safety; R0040396:Abstract |
Discontinuation due to gastrointestinal adverse events (3 lines; O27E)
| Week | Arm | Statistic | Estimate | SE or SD | 95% CI | Events / N | Detail |
|---|---|---|---|---|---|---|---|
| A1 | events | 3 / 38 | not stated; safety; R0040396:Table 3 | ||||
| A1 vs A2 | or | 1.67 | not stated; safety; R0040396:Table 3 | ||||
| A2 | events | 2 / 41 | not stated; safety; R0040396:Table 3 |