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Comparison · NCT03065244-deaths

IVIG vs Infliximab: deaths from any cause

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. IVIG vs Infliximab: deaths from any cause. Trial comparisons, record NCT03065244-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03065244-deaths

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 100.000000000000000006940.0727wilson
Risk in group 2000.0664wilson
Risk difference, group 1 minus group 20-0.06640.0727newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1IVIGPatient will be randomly assigned to receive a second IVIG infusion: 2 g/kg IV over 8-10 hours single infusion~IVIG: Subjects randomized to this arm will receive IVIG 2g/kg over 10-12 hours049EG000
Group 2InfliximabPatient will be randomly assigned to receive Infliximab 10 mg/kg IV over 2 hours~Infliximab: Subjects randomized to this arm will receive infliximab 10 mg/kg over 2 hours054EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse event data were collected during the entirety of the study participation which was 6 weeks from study enrollment.

Source ClinicalTrials.gov

Trial

Title
KIDCARE (Kawasaki Disease Comparative Effectiveness Trial)
NCT number
NCT03065244
Phases
PHASE3
Conditions
Mucocutaneous Lymph Node Syndrome
Interventions
IVIG, Infliximab
Lead sponsor
University of California, San Diego
Results first posted
2021-12-03

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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