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Comparison · NCT03058666-e31597bd

Aerosolized Calfactant vs Usual Care: Respiratory Support Requirements

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. Aerosolized Calfactant vs Usual Care: Respiratory Support Requirements. Trial comparisons, record NCT03058666-e31597bd. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03058666-e31597bd

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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 10.270.2180.329wilson
Risk in group 20.5250.4620.588wilson
Risk difference, group 1 minus group 2-0.256-0.337-0.169newcombe hybrid score
Risk ratio, group 1 over group 20.5130.4040.653log
Odds ratio, group 1 over group 20.3340.2280.489log
Number needed to treat, for one fewer participant with the outcome on Aerosolized Calfactant than on Usual Care3.912.965.93from the risk difference interval

Groups2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Aerosolized CalfactantAerosolized Calfactant: Aerosolization of Infasurf at 6ml/kg via the modified Solarys aerosol generator.~Solarys: Aerosolization of Infasurf at 6ml/kg via the modified Solarys aerosol generator.65241OG000
Group 2Usual CareThere will be no protocol driven interventions in the usual care group.124236OG001

Outcome

Type
SECONDARY
Title
Respiratory Support Requirements
Description
Difference of Respiratory support at 28 days
Time frame
28 days
Population

Source ClinicalTrials.gov

Trial

Title
Comparison of Aerosol Delivery of Infasurf to Usual Care in Spontaneously Breathing RDS Patients
NCT number
NCT03058666
Phases
PHASE3
Conditions
Respiratory Distress Syndrome
Interventions
Aerosolized Calfactant, Solarys
Lead sponsor
ONY
Results first posted
2024-05-29

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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