LivingGLP1
Descriptive only

Percent body weight change

Children and adolescents with obesity

weeks 20 to 40 (target week 26)Not stated by the trialsEach dose separatelyMean difference
1
Randomized trials
2
Treatments
251
Participants
2
Trial arms

In plain language

No network meta-analysis was fitted here. The protocol requires at least two trials forming a connected network; this outcome has 1 trial. The trial data below are shown as reported.

Network of trials

Each circle is a treatment; each line joins treatments that were randomized against each other in at least one trial.
LIRA_SC_3p0MG_QDPLACEBO
Node area shows participants; line width shows trials comparing two treatments directly. Blue: GLP-1 receptor agonist containing treatments; grey: comparators. Hover over or tab to a node or line for details.

Baseline characteristics of the trials

The baseline value of each effect modifier or prognostic factor that applies here, per trial: mean or percent over arms, weighted by the number randomized. A note under a value names a stand in (a median for a mean, 100 minus the male share, Asian subgroup rows, an all Asian site list); "not reported" means no source of the trial prints it.
Baseline effect modifiers and prognostic factors per trial
TrialBaseline BMI or body weight (kg/m2)
effect modifier, prognostic factor; 1 of 1
Sex (percent female)
effect modifier, prognostic factor; 1 of 1
Asian ancestry or region (percent Asian)
effect modifier, prognostic factor; 1 of 1
Treatment duration (weeks)
effect modifier; 1 of 1
Lifestyle co-intervention intensity (none standard intensive)
effect modifier, prognostic factor; 1 of 1
NCT02918279
S000599
35.5559.360.856standard

Comparability of the trials

Checked across designs (the set of treatments each trial compares) for eligibility, outcome definition and assessment, and the baseline factors above. Flags point to possible intransitivity; notes describe variation that is not tied to design.

No comparability concerns were found.

Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT0291827930full_analysisnot statednot statednot statednot statednot statednot stateddouble_blindindustry2016pubertal age 12 to under 18; BMI equivalent to adult 30 or more; poor response to lifestyle therapy

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the mean difference on the analysis scale against the trial's first row. Flags mark converted, combined or approximated inputs.
Trial data entering this analysis
TrialArmTreatmentWeekDataValueSEEvents / NFlagsSource
NCT02918279A1LIRA_SC_3p0MG_QD30arm, percent_change-4.3000.581125registry:outcomes
NCT02918279A2PLACEBO30arm, percent_change0.4000.552126registry:outcomes

Rerun this analysis yourself

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