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Open Group vs Masked Group: Number of Participants Experiencing Postpartum Endometritis

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 10.01280.01020.0162wilsonClinicalTrials.gov
Risk in group 20.01580.01280.0194wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00295-0.007430.0015newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.8130.5961.11logClinicalTrials.gov
Odds ratio, group 1 over group 20.8110.5921.11logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Open Group than on Masked Group339from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Open Group
• Fetal STAN monitor electrode inserted and data available to caregivers~fetal STAN monitor: The STAN monitor is a system for fetal surveillance that displays the FHR, the uterine activity and information resulting from the analysis of the ST segment of the fetal ECG.
715,532OG000ClinicalTrials.gov
Group 2Masked Group
•Fetal STAN monitor electrode inserted, but data masked to the caregivers~fetal STAN monitor: The STAN monitor is a system for fetal surveillance that displays the FHR, the uterine activity and information resulting from the analysis of the ST segment of the fetal ECG.
885,576OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants Experiencing Postpartum EndometritisClinicalTrials.gov
DescriptionPostpartum endometritisClinicalTrials.gov
Time frameDelivery through hospital dischargeClinicalTrials.gov
PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleFetal ST Segment and T Wave Analysis in LaborClinicalTrials.gov
NCT numberNCT01131260ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsPregnancy, Obstetric Labor, ParturitionClinicalTrials.gov
Interventionsfetal STAN monitorClinicalTrials.gov
Lead sponsorThe George Washington University Biostatistics CenterClinicalTrials.gov
Results first posted2019-04-05ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01131260?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.