LivingGLP1
parallel randomized trial

S002938

Design

Randomized
84
Start year
2017
Treatment
12 weeks, follow-up 12 weeks
Countries
China (1 sites)
Sponsor
(non industry)
Eligibility
age 18 to 65; GLP-1RA naive; diabetic nephropathy

Conduct and analysis

Blinding
not reported
Sequence generation
other adequate
Allocation concealment
not reported
Outcome adjudication
not reported
Primary estimand
not stated
Analysis population
Missing data

Arms

ArmTreatmentBackgroundRandomizedAnalyzedCompleted treatment
A1Standard care or no added treatment
Conventional treatment
diet, exercise education, oral drugs or insulin, blood pressure and lipid treatment; lifestyle: standard4242
A2Liraglutide subcutaneous once daily, flexible dose: 1.2 or 1.8 mg by tolerability
Liraglutide plus conventional treatment
diet, exercise education, oral drugs or insulin, blood pressure and lipid treatment; lifestyle: standard4242

Baseline characteristics

As printed in the trial reports or registry, per arm or for the whole trial.
CharacteristicStatisticStandard care or no added treatment
A1
Liraglutide subcutaneous once daily, flexible dose: 1.2 or 1.8 mg by tolerability
A2
agemax (years)6365
agemean (years)45.3846.89
agemin (years)3638
agesd (years)10.3411.26
bmimean (kg/m2)27.4227.83
bmisd (kg/m2)2.212.71
diabetes durationmean (years)9.3710.04
diabetes durationsd (years)5.816.12
femalen2021
hba1cmean (percent)9.819.98
hba1csd (percent)0.960.87
other uaermean (μg/min)288.62282.47
other uaersd (μg/min)32.2431.86

Results

2 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
HbA1c change (2 lines; O01)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
12A1final7.16 percent0.6242not stated; other; R0005474:Table I
12A2final6.45 percent0.5142not stated; other; R0005474:Table I