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Conventional vs suPAR: Number of Readmissions

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 10.0870.08090.0934wilsonClinicalTrials.gov
Risk in group 20.1030.09690.11wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0161-0.0249-0.0072newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.8440.7680.927logClinicalTrials.gov
Odds ratio, group 1 over group 20.8290.7470.92logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Conventional than on suPAR62.240.1139from the risk difference intervalClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Conventionalno suPAR measurement. Standard care.6877,901OG000ClinicalTrials.gov
Group 2suPAR
suPAR measurement and education of doctors working in the Emergency department in the meaning of low or elevated levels of suPAR. Since suPAR is measured on all patients regardless of disease the investigators cannot define a single intervention. A possible intervention depends on the clinical situation.~suPAR measurement: The biomarker suPAR will be measured on all patients included in the study. Before the study period the doctors will receive information on suPAR. We want to study if the information provided by suPAR is useful in emergency medicine. Interventions depends on the clinical issue, as suPAR is an unspecific marker of disease. Usually a elevated suPAR level could result in more investigation e.g. diagnostic procedures or follow up, while a low suPAR could result in faster discharge.
9178,900OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of ReadmissionsClinicalTrials.gov
DescriptionPatients will be followed using central registers. All new admissions within 90 days of the same patient is defined as readmissions.ClinicalTrials.gov
Time frame90 daysClinicalTrials.gov
PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleRisk Stratification in Acute Care: The Meaning of suPAR Measurement in TriageClinicalTrials.gov
NCT numberNCT02643459ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsTriage, Risk Stratification With BiomarkerClinicalTrials.gov
InterventionssuPAR measurementClinicalTrials.gov
Lead sponsorHerlev HospitalClinicalTrials.gov
Results first posted2021-03-09ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02643459?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.