LivingGLP1
parallel randomized trial

S003014

Design

Randomized
115
Start year
Treatment
26.07 weeks, follow-up 26.07 weeks
Countries
Ukraine (1 sites)
Sponsor
(not reported)
Eligibility
age 26 to 67; MASLD by steatometry with a cardiometabolic risk factor; no prior cardiovascular events or cirrhosis

Conduct and analysis

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

Arms

ArmTreatmentBackgroundRandomizedAnalyzedCompleted treatment
A1Standard care or no added treatment
Control, lifestyle only
Mediterranean diet and at least 150 minutes weekly moderate activity; lifestyle: standard3636
A2Dapagliflozin
Dapagliflozin (Group IA)
Mediterranean diet and 150 min weekly moderate activity; lifestyle: standard4141
A3Liraglutide 1.8 mg subcutaneous once daily
Liraglutide (Group IB)
Mediterranean diet and 150 min weekly moderate activity; lifestyle: standard3838

Baseline characteristics

As printed in the trial reports or registry, per arm or for the whole trial.
CharacteristicStatisticStandard care or no added treatment
A1
Dapagliflozin
A2
Liraglutide 1.8 mg subcutaneous once daily
A3
age: 25 to 34n81210
age: 25 to 34percent22.229.326.3
age: 35 to 44n111313
age: 35 to 44percent30.631.734.2
age: 45 to 54n12109
age: 45 to 54percent33.324.423.7
age: 55 to 67n566
age: 55 to 67percent13.914.615.8
agemean (years)43.341.739.6
agesd (years)1110.711.2
bmimean (kg/m2)30.9531.6132.16
bmisd (kg/m2)3.43.14.4
femalen11178
femalepercent314121
sbpmean (mmHg)132.5133.7132.2
sbpsd (mmHg)13.616.615.6