After gastric bypass, dasiglucagon reduced time in level 1 hypoglycemia by 33% versus placebo, a -1.2 percentage point difference, P = 0.002.
In plain wordsAfter gastric bypass, dasiglucagon reduced time in level 1 hypoglycemia by 33% compared with placebo.
- Peptide
- Dasiglucagon
- Outcome
- DecreaseTime in level 1 hypoglycemia
- Study
n = 24
- Comparator
- Placebo
- Analysis
- Primary
- Outcome group
- Glycemic control · Metabolic and weight
- Studied dose
- 120 μg · subcutaneous · 4 weeksAs given in this study (human).
Measurements
- Relative reduction
- 33%
- level 1 hypoglycemia
- Difference
- −1.2 percentage points
- versus placebo
- 95% CI
- −2 to −0.5 percentage points
- difference
Source sentences
Compared with placebo, treatment with dasiglucagon significantly reduced time in level 1 hypoglycemia by 33% (-1.2 percentage points; 95% CI -2.0 to -0.5; P = 0.002) and time in level 2 hypoglycemia by 54% (-0.4 percentage points; 95% CI -0.6 to -0.2; P < 0.0001).
4 context sentences(design, population, supporting numbers)
The primary and key secondary outcomes were continuous glucose monitor-captured percentage of time in level 1 and 2 hypoglycemia (<3.9 and <3.0 mmol/L), respectively.
We conducted a randomized, double-blind, placebo-controlled, crossover, proof-of-concept study at the Center for Clinical Metabolic Research at Gentofte Hospital in Denmark.
The study included 24 individuals who had undergone Roux-en-Y gastric bypass surgery (n = 23 women)
randomly assigned to two treatment periods of 4 weeks of self-administered subcutaneous dasiglucagon at 120 μg or placebo.