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Phase I: Observational, Mother vs Phase I: Observational, Neonate: deaths from any cause

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.0004210.0001430.00124wilsonClinicalTrials.gov
Risk in group 20.06160.05630.0673wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0611-0.0669-0.0558newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.006830.00220.0213logClinicalTrials.gov
Odds ratio, group 1 over group 20.006420.002060.02logClinicalTrials.gov
Number needed to treat, for one fewer death from any cause on Phase I: Observational, Mother than on Phase I: Observational, Neonate16.41517.9from the risk difference intervalClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Phase I: Observational, MotherMother enrolled from the two participating hospitals and completed the 6-week follow-up37,131EG000ClinicalTrials.gov
Group 2Phase I: Observational, NeonateNeonate enrolled after delivery and completed the 6-week follow-up4537,359EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, all-cause mortalityClinicalTrials.gov
Time frameClinicalTrials.gov

Trial 8

FieldValueSource
TitleSmart Discharges for Mom & BabyClinicalTrials.gov
NCT numberNCT05730387ClinicalTrials.gov
PhasesClinicalTrials.gov
ConditionsMaternal Sepsis, Neonatal SepsisClinicalTrials.gov
InterventionsObservational onlyClinicalTrials.gov
Lead sponsorUniversity of British ColumbiaClinicalTrials.gov
Results first posted2025-04-10ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT05730387?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.