LivingGLP1
Descriptive only

Four point MACE including unstable angina

Type 2 diabetes (adults)

longest follow-upCause specific hazardsDoses of a drug pooledHazard ratio
1
Randomized trials
2
Treatments
0
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.
ALBI_SCPLACEBO
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
TrialAge (years)
prognostic factor; 1 of 1
Established cardiovascular disease (percent of participants)
prognostic factor; 0 of 1
Kidney function (eGFR) (mL/min/1.73 m2)
prognostic factor, effect modifier; 0 of 1
NCT02465515
S001074
64.15not reportednot reported

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.
  • FlagBaseline, Established cardiovascular disease: not reported by 1 of 1 trials
  • FlagBaseline, Kidney function (eGFR): not reported by 1 of 1 trials
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT02465515140.89randomizednot statednot statednot statednot statednot statednot stateddouble_blindindustry2015type 2 diabetes with established cardiovascular disease

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the hazard ratio on the analysis scale (log) against the trial's first row. Flags mark converted, combined or approximated inputs.
Trial data entering this analysis
TrialArmTreatmentWeekDataValueSEEvents / NFlagsSource
NCT02465515A1PLACEBO140.89contrast, hrregistry:outcomes
NCT02465515A2ALBI_SC140.89contrast, hr-0.2480.068registry:outcomes

Rerun this analysis yourself

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