LivingGLP1
Descriptive only

Weight loss of 5 percent or more

Type 2 diabetes (adults); background therapy: one or more non insulin glucose lowering drugs

weeks 20 to 40 (target week 26)Not stated by the trialsEach dose separatelyOdds ratioSeparate part 3 of a disconnected network
1
Randomized trials
3
Treatments
685
Participants
153
Events

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.
DAPAEXEN_SC_2-10MG_QWDAPAGLIFLOZINEXENER_SC_2MG_QW
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
Treatment duration (weeks)
effect modifier; 1 of 1
Lifestyle co-intervention intensity (none standard intensive)
effect modifier, prognostic factor; 1 of 1
NCT02229396
S000791
32.7352104not_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.
  • NoteData handling, input conversions: count_from_percent 3
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT0222939628modified_ittHbA1c below 7 percent at week 28not statednot statednot_statednot statednot stateddouble_blindindustry2014age 18 or older; HbA1c 8.0 to 12.0 percent on metformin 1500 mg/d or more

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the odds 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
NCT02229396A1DAPAEXEN_SC_2-10MG_QW28arm, responders76 / 228count_from_percentregistry:outcomes
NCT02229396A2EXENER_SC_2MG_QW28arm, responders31 / 227count_from_percentregistry:outcomes
NCT02229396A3DAPAGLIFLOZIN28arm, responders46 / 230count_from_percentregistry:outcomes

Rerun this analysis yourself

Remove treatments or trials and refit the frequentist and Bayesian models in your browser, with the same methods as the published analysis.

Open in the NMA lab