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Comparison · NCT01353313-sae

Hydrocortisone vs Placebo: serious adverse events

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. Hydrocortisone vs Placebo: serious adverse events. Trial comparisons, record NCT01353313-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01353313-sae

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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 10.2110.1740.254wilson
Risk in group 20.2360.1970.28wilson
Risk difference, group 1 minus group 2-0.0253-0.08280.0325newcombe hybrid score
Risk ratio, group 1 over group 20.8930.6891.16log
Odds ratio, group 1 over group 20.8640.621.21log
Number needed to treat, for one fewer participant with a serious adverse event on Hydrocortisone than on Placebo39.6from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1HydrocortisoneHydrocortisone sodium succinate administered intravenously or orally if no intravenous line was available, tapered over 10 days.84398EG000
Group 2PlaceboSaline placebo administered intravenously or orally if no intravenous line was available.95402EG001

Harm

What it counts
Total, serious adverse events
Time frame
Birth to 36 weeks PMA

Source ClinicalTrials.gov

Trial

Title
Hydrocortisone for BPD
NCT number
NCT01353313
Phases
PHASE3
Conditions
Infant, Newborn, Infant, Small for Gestational Age, Infant, Very Low Birth Weight, Infant, Premature, Bronchopulmonary Dysplasia
Interventions
Hydrocortisone, Placebo
Lead sponsor
NICHD Neonatal Research Network
Results first posted
2022-08-19

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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