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Comparison · NCT01004029-ecee4993

17P (Hydroxyprogesterone Caproate Injection) vs Vehicle: Neonatal Deaths With ≥24 Weeks Gestational Age

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. 17P (Hydroxyprogesterone Caproate Injection) vs Vehicle: Neonatal Deaths With ≥24 Weeks Gestational Age. Trial comparisons, record NCT01004029-ecee4993. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01004029-ecee4993

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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 10.002740.0009340.00804wilson
Risk in group 20.003580.0009830.013wilson
Risk difference, group 1 minus group 2-0.000839-0.01040.00506newcombe hybrid score
Risk ratio, group 1 over group 20.7660.1284.57log
Odds ratio, group 1 over group 20.7650.1274.59log
Number needed to treat, for one fewer participant with the outcome on 17P (Hydroxyprogesterone Caproate Injection) than on Vehicle1,190from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: vehicle.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 117P (Hydroxyprogesterone Caproate Injection)HPC 250 mg/mL in oil~Hydroxyprogesterone Caproate Injection, 250mg/mL: 1 mL intramuscular injection every week until 36 weeks, 6 days of gestation or delivery, whichever occurs first.31,093OG001
Group 2VehicleCastor Oil~Vehicle: Weekly intramuscular injections of 1 mL vehicle inert oil until 36 weeks, 6 days of gestation or delivery, whichever occurs first.2558OG000

Outcome

Type
SECONDARY
Title
Neonatal Deaths With ≥24 Weeks Gestational Age
Description
Neonatal death (from minutes after birth until 28 days of life) occurring in liveborns born at 24 weeks gestation or greater
Time frame
Until 28 days of life or discharge from the NICU whichever occurred later.
Population
Liveborn Neonatal Population - all babies of randomized women who were liveborn and have morbidity data available.

Source ClinicalTrials.gov

Trial

Title
Confirmatory Study of 17P vs Vehicle for Prevention of Preterm Birth in Women w/ Previous Spontaneous Preterm Delivery
NCT number
NCT01004029
Phases
PHASE3
Conditions
Preterm Birth
Interventions
Hydroxyprogesterone Caproate Injection (HPC), 250mg/mL, Vehicle
Lead sponsor
AMAG Pharmaceuticals, Inc.
Results first posted
2021-01-28

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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