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Comparison · NCT00179777-deaths

Nonhydrolysed Infant Formula vs Hydrolysed Infant Formula: 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. Nonhydrolysed Infant Formula vs Hydrolysed Infant Formula: deaths from any cause. Trial comparisons, record NCT00179777-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00179777-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 10.004640.001980.0108wilson
Risk in group 20.004630.001980.0108wilson
Risk difference, group 1 minus group 20.0000129-0.006690.00673newcombe hybrid score
Risk ratio, group 1 over group 210.2913.45log
Odds ratio, group 1 over group 210.2893.47log
Number needed to harm, for one more death from any cause on Nonhydrolysed Infant Formula than on Hydrolysed Infant Formula77,700from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Nonhydrolysed Infant FormulaReported Adverse Events during the Follow-up in the Nonhydrolysed Infant Formula Group51,078EG000
Group 2Hydrolysed Infant FormulaReported Adverse Events during the Follow-up in the Hydrolysed Infant Formula Group51,081EG001

Harm

What it counts
Total, all-cause mortality
Time frame
11.5 years

Source ClinicalTrials.gov

Trial

Title
TRIGR - Primary Prevention Study for Type 1 Diabetes in Children at Risk
NCT number
NCT00179777
Phases
NA
Conditions
Diabetes Mellitus, Type 1
Interventions
Hydrolysed infant formula, Nonhydrolysed infant formula
Lead sponsor
University of Helsinki
Results first posted
2021-07-30

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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