LivingGLP1
parallel randomized trial

S003034

Design

Randomized
52
Start year
Treatment
6 weeks, follow-up 6 weeks
Countries
Denmark (2 sites)
Sponsor
(mixed)
Eligibility
SeHCAT 10 percent or less; no diabetes; bile acid diarrhea

Conduct and analysis

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

Arms

ArmTreatmentBackgroundRandomizedAnalyzedCompleted treatment
A1Liraglutide 1.8 mg subcutaneous once daily
Liraglutide 1.8 mg daily
lifestyle: not reported26
A2Colesevelam
Colesevelam 1875 mg twice daily
lifestyle: not reported26

Baseline characteristics

As printed in the trial reports or registry, per arm or for the whole trial.
CharacteristicStatisticLiraglutide 1.8 mg subcutaneous once daily
A1
Colesevelam
A2
Whole trial
ALL
agemean (years)51.748.7
agesd (years)13.312.8
bmimean (kg/m2)31.528.3
bmisd (kg/m2)5.64.1
femalen32

Results

4 adjudicated result lines, grouped by outcome. Open an outcome to see its values.
Discontinuation due to adverse events (2 lines; O26)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events1 / 26not stated; randomized; R0018327:Results
A2events1 / 26not stated; randomized; R0018327:Results
Discontinuation due to gastrointestinal adverse events (2 lines; O27E)
WeekArmStatisticEstimateSE or SD95% CIEvents / NDetail
A1events1 / 26not stated; randomized; R0018327:Results
A2events1 / 26not stated; randomized; R0018327:Results