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No PN Use (Project B) vs PN Use (Project B): Need for Surgical Procedures (Project B)

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 10.008470.00670.0107wilsonClinicalTrials.gov
Risk in group 20.0180.01540.0212wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00958-0.0132-0.00609newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.4690.3530.624logClinicalTrials.gov
Odds ratio, group 1 over group 20.4650.3490.62logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on No PN Use (Project B) than on PN Use (Project B)10475.9164from 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 1No PN Use (Project B)
All neonates born between 30 and 33 weeks postmenstrual age in England and Wales and admitted to a NHS neonatal unit between 1st January 2012 and 31st December 2017 who did not receive any parenteral nutrition (for any duration, by any intravenous route) in the first seven postnatal days.
698,146OG000ClinicalTrials.gov
Group 2PN Use (Project B)
All neonates born between 30 and 33 weeks postmenstrual age in England and Wales and admitted to a NHS neonatal unit between 1st January 2012 and 31st December 2017 who received any parenteral nutrition (for any duration, by any intravenous route) in the first seven postnatal days.~Parenteral nutrition: Parenteral nutrition is the administration of an intravenous solution containing amino acids (with or without lipids) to provide nutritional support.
1478,146OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNeed for Surgical Procedures (Project B)ClinicalTrials.gov
DescriptionDefined as any record of surgical procedure during the neonatal admissionClinicalTrials.gov
Time frameFrom birth until discharge home, assessed up to 1 yearClinicalTrials.gov
PopulationAnalysis of propensity score matched cohorts as per the pre-specified analysis planClinicalTrials.gov

Trial 8

FieldValueSource
TitleOutcomes Following Early Parenteral Nutrition Use in Preterm NeonatesClinicalTrials.gov
NCT numberNCT03767634ClinicalTrials.gov
PhasesClinicalTrials.gov
ConditionsNeonatal Death, PrematurityClinicalTrials.gov
InterventionsParenteral nutritionClinicalTrials.gov
Lead sponsorImperial College LondonClinicalTrials.gov
Results first posted2022-03-17ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT03767634?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.