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Comparison · NCT04026555-dc36fb66

Intervention - Alert Sent vs Control - No Alert Sent: Number of Participants Requiring Blood Pressure Support

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 - Alert Sent vs Control - No Alert Sent: Number of Participants Requiring Blood Pressure Support. Trial comparisons, record NCT04026555-dc36fb66. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04026555-dc36fb66

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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 10.1610.1430.18wilson
Risk in group 20.1130.0970.132wilson
Risk difference, group 1 minus group 20.04720.02140.0727newcombe hybrid score
Risk ratio, group 1 over group 21.421.171.72log
Odds ratio, group 1 over group 21.51.21.87log
Number needed to treat, for one more participant with the outcome on Intervention - Alert Sent than on Control - No Alert Sent21.213.846.8from the risk difference interval

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Intervention - Alert Sent
A score predicting the likelihood that the patient will experience a deterioration in their clinical condition within six hours will be generated. If the prediction score exceeds a predetermined threshold, an alert will be sent to the provider. The alerting protocol is tiered, with both a low and high threshold. If the score is above the low threshold, nursing will be notified. If the score is above the high threshold, RRT will be notified.
2391,488OG000
Group 2Control - No Alert Sent
A score predicting the likelihood that the patient will experience a deterioration in their clinical condition within six hours will be generated. Patients in the control arm will have a score calculated but no alert will be sent.
1421,252OG001

Outcome

Type
SECONDARY
Title
Number of Participants Requiring Blood Pressure Support
Description
Number of participants requiring blood pressure support agents such as initiation of vasopressor medication or administration of fluid bolus.
Time frame
10 months
Population

Source ClinicalTrials.gov

Trial

Title
Realtime Streaming Clinical Use Engine for Medical Escalation
NCT number
NCT04026555
Phases
NA
Conditions
Clinical Deterioration, Hospital Medicine, Monitoring, Physiologic
Interventions
MEWS++ Monitoring, Predictor Score
Lead sponsor
Icahn School of Medicine at Mount Sinai
Results first posted
2025-01-14

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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