LivingGLP1
Descriptive only

HbA1c change

Children and adolescents with type 2 diabetes

weeks 12 to 40 (target week 26)Hypothetical (as if everyone stayed on treatment)Each dose separatelyMean difference
1
Randomized trials
2
Treatments
82
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.
EXENER_SC_2MG_QWPLACEBO
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 HbA1c (percent)
effect modifier, prognostic factor; 1 of 1
Asian ancestry or region (percent Asian)
effect modifier, prognostic factor; 1 of 1
Age (years)
prognostic factor; 1 of 1
Treatment duration (weeks)
effect modifier; 1 of 1
NCT01554618
S000457
8.163.6315.2952

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
Trialfundingtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingstart yearEligibility
NCT01554618industry24modified_ittnot statednot statednot statednot statedhypotheticalhypotheticaldouble_blind2011age 10 to below 18; HbA1c 6.5 to 11.0 (12.0 if insulin or sulfonylurea)

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
NCT01554618A1EXENER_SC_2MG_QW24arm, change-0.3600.18458R0017380:Results
NCT01554618A2PLACEBO24arm, change0.4900.27324R0017380:Results

Rerun this analysis yourself

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