LivingGLP1
parallel randomized trial

S003022

Design

Randomized
60
Start year
2018
Treatment
12 weeks, follow-up 12 weeks
Countries
China (1 sites)
Sponsor
(non industry)
Eligibility
women with PCOS (Rotterdam); age over 18; premenopausal; BMI 24 or more

Conduct and analysis

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

Arms

ArmTreatmentBackgroundRandomizedAnalyzedCompleted treatment
A1Metformin
Metformin (MET)
lifestyle: not reported2019
A2Liraglutide 1.2 mg subcutaneous once daily
LIRA
lifestyle: not reported2018
A3Liraglutide and metformin 1.2 to 0.85 mg injection once daily
Liraglutide plus metformin (COM)
lifestyle: not reported2017

Baseline characteristics

As printed in the trial reports or registry, per arm or for the whole trial.
CharacteristicStatisticMetformin
A1
Liraglutide 1.2 mg subcutaneous once daily
A2
Liraglutide and metformin 1.2 to 0.85 mg injection once daily
A3
Whole trial
ALL
bmimean (kg/m2)28.1027.9426.68
bmisd (kg/m2)2.952.592.14
femalen60
hba1cmean (percent)5.355.285.26
hba1csd (percent)0.380.400.34
weightmean (kg)69.2067.5169.24
weightsd (kg)8.327.697.72

Analyses this trial contributes to

Results

19 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
Percent body weight change (short trials) (3 lines; O10B)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
12A1percent change-5.28 percent19not stated; completers; R0015954:Results
12A2percent change-7.71 percent18not stated; completers; R0015954:Results
12A3percent change-10.55 percent17not stated; completers; R0015954:Results
Discontinuation due to adverse events (3 lines; O26)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events1 / 20not stated; randomized; R0015954:Figure 1
A2events2 / 20not stated; randomized; R0015954:Figure 1
A3events3 / 20not stated; randomized; R0015954:Figure 1
Nausea (3 lines; O27A)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events6 / 19not stated; completers; R0015954:Results
A2events9 / 18not stated; completers; R0015954:Results
A3events9 / 17not stated; completers; R0015954:Results
Vomiting (3 lines; O27B)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events4 / 19not stated; completers; R0015954:Results
A2events3 / 18not stated; completers; R0015954:Results
A3events5 / 17not stated; completers; R0015954:Results
Diarrhea (3 lines; O27C)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events4 / 19not stated; completers; R0015954:Results
A2events4 / 18not stated; completers; R0015954:Results
A3events6 / 17not stated; completers; R0015954:Results
Constipation (1 lines; O27D)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A3events1 / 17not stated; completers; R0015954:Results
Discontinuation due to gastrointestinal adverse events (3 lines; O27E)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events1 / 20not stated; randomized; vomiting; R0015954:Figure 1
A3events1 / 20not stated; randomized; diarrhea; R0015954:Figure 1
A3events2 / 20not stated; randomized; vomiting; R0015954:Figure 1