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Appy CDS Intervention vs Control: serious adverse events

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 10.03040.02490.0369wilsonClinicalTrials.gov
Risk in group 20.03920.03260.0471wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00885-0.01840.000467newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.7740.5911.01logClinicalTrials.gov
Odds ratio, group 1 over group 20.7670.581.01logClinicalTrials.gov
Number needed to treat, for one fewer participant with a serious adverse event on Appy CDS Intervention than on Control113from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Appy CDS Intervention
The Appy-cds intervention is a point of care clinical decision support system designed to identify pediatric patients at risk for appendicitis using EHR and supplemental data. The Appy-cds has multiple components, 1) presents risk prediction/stratification to provider, 2) provides recommendations consistent with standardized appendicitis care, 3) alerts for unnecessary exposure to ionizing radiation via a best practice alert. The intervention is administered to providers in this arm.~Post Appy Clinical Decision Support: The Appy CDS is a point of care clinical decision support system that provides the provider with 1) risk for appendicitis based on EHR data, 2) recommendations on actions to take based on risk, 3) advises on imaging use.
963,161EG000ClinicalTrials.gov
Group 2ControlPeople in the control arm receive usual care.1092,779EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, serious adverse eventsClinicalTrials.gov
Time frameWithin 7 days of index ED visit.ClinicalTrials.gov

Trial 8

FieldValueSource
TitleEHR-based Decision Support for Pediatric Acute Abdominal Pain in Emergency CareClinicalTrials.gov
NCT numberNCT02633735ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsAppendicitisClinicalTrials.gov
InterventionsAppy CDSClinicalTrials.gov
Lead sponsorHealthPartners InstituteClinicalTrials.gov
Results first posted2020-07-09ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02633735?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.