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Comparison · NCT04060667-deaths

Intervention vs Control: deaths from any cause

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. Intervention vs Control: deaths from any cause. Trial comparisons, record NCT04060667-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04060667-deaths

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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 10.001930.0006580.00567wilson
Risk in group 20.0006140.0001080.00347wilson
Risk difference, group 1 minus group 20.00132-0.001810.00509newcombe hybrid score
Risk ratio, group 1 over group 23.150.32830.2log
Odds ratio, group 1 over group 23.150.32830.3log
Number needed to harm, for one more death from any cause on Intervention than on Control758from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Intervention
Wireless physiologic monitoring: The intervention in this study is the use of a wireless monitor to perform physiologic monitoring of women undergoing emergency cesarean delivery for the first 24 hours after completion of the cesarean and send alerts to responding clinicians should vital signs fall out of a pre-specified range.
31,552EG000
Group 2ControlStandard of Care monitoring11,629EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Until hospital discharge, an average of 3 days

Source ClinicalTrials.gov

Trial

Title
Wireless Physiologic Monitoring in Postpartum Women
NCT number
NCT04060667
Phases
NA
Conditions
Maternal Death During Childbirth, Pregnancy Complications
Interventions
Wireless physiologic monitoring
Lead sponsor
Massachusetts General Hospital
Results first posted
2025-09-09

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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