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Electronic AKI Alert vs Usual Care: Composite of Progression of AKI, Inpatient Dialysis, or Inpatient Death

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 10.2130.1990.228wilsonClinicalTrials.gov
Risk in group 20.2090.1950.224wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.00411-0.01650.0247newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.020.9251.12logClinicalTrials.gov
Odds ratio, group 1 over group 21.020.9061.16logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Electronic AKI Alert than on Usual Care243from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Electronic AKI Alert
A pop-up alert will fire when a provider opens the electronic health record of a patient with AKI until such time as AKI is documented in the problem list, or AKI resolves.~AKI Alert: Provider's will receive a pop-up alert in the electronic health record until AKI is documented in the problem list or AKI resolves.
6533,059OG001ClinicalTrials.gov
Group 2Usual CareNo alert will be fired.6222,971OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleComposite of Progression of AKI, Inpatient Dialysis, or Inpatient DeathClinicalTrials.gov
Description
Progression of AKI is defined by an increase in KDIGO creatinine stage from that present at the time of randomization.~Dialysis is defined by the receipt of hemodialysis, continuous renal replacement therapy or peritoneal dialysis. Isolated ultrafiltration treatments (for the purpose of volume removal) will not be included.~Mortality will be determined from hospital administrative records.
ClinicalTrials.gov
Time frame14 days from randomizationClinicalTrials.gov
PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleOptimizing Electronic Alerts for Acute Kidney InjuryClinicalTrials.gov
NCT numberNCT02753751ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsAcute Kidney InjuryClinicalTrials.gov
InterventionsAKI AlertClinicalTrials.gov
Lead sponsorYale UniversityClinicalTrials.gov
Results first posted2022-02-10ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02753751?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.