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Trial · NCT01422070

European Mortality & Length Of Intensive Care Unit (ICU) Stay Evaluation (ELOISE)

NCT01422070, Completed, Università degli Studi di Ferrara; results first posted 2015-03-02

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. European Mortality & Length Of Intensive Care Unit (ICU) Stay Evaluation (ELOISE). Trials, record NCT01422070. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01422070

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
European Mortality & Length Of Intensive Care Unit (ICU) Stay Evaluation (ELOISE)
NCT number
NCT01422070
Status
Completed
Enrollment
6,433 participants, actual
Lead sponsor
Università degli Studi di Ferrara
Conditions
Critical Illness
First posted
2011-08-23
Last updated
2015-08-21
Results first posted
2015-03-02

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryVital Status at Hospital DischargeMax 90 days after admission to the Study UnitHospital mortality of the patients admitted to intensive care units with or without intermediate care unit in the hospital
SecondaryLength of ICU StayMax 90 days after admission to intensive care unitNumber of days (calendar days -1) from admission to and discharge from the Study Unit
SecondaryLength of Hospital StayMax 90 days after admission to the Study UnitNumber of days (calendar days -1) from admission to the Study Unit to discharge from the hospital
SecondaryNumber of ICU ReadmissionsMax 90 days after admission to the Study UnitNumber of readmissions to intensive care unit during the same hospital course

Outcomes4

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYVital Status at Hospital DischargeMax 90 days after admission to the Study UnitparticipantsNUMBER
SECONDARYLength of ICU StayMax 90 days after admission to intensive care unitdaysMEDIAN
SECONDARYLength of Hospital StayMax 90 days after admission to the Study UnitdaysMEDIAN
SECONDARYNumber of ICU ReadmissionsMax 90 days after admission to the Study UnitreadmissionsNUMBER

Results by group8

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Vital Status at Hospital DischargeUnits in Hospitals With Intermediate Care Unit1232participants
Vital Status at Hospital DischargeUnits in Hospitals Without Intermediate Care Unit165participants
Length of ICU StayUnits in Hospitals With Intermediate Care Unit3.7Inter-Quartile Range 1.9 to 7.7days
Length of ICU StayUnits in Hospitals Without Intermediate Care Unit2.8Inter-Quartile Range 1.8 to 4.8days
Length of Hospital StayUnits in Hospitals With Intermediate Care Unit13.9Inter-Quartile Range 7.6 to 25.0days
Length of Hospital StayUnits in Hospitals Without Intermediate Care Unit11.0Inter-Quartile Range 6.2 to 11.0days
Number of ICU ReadmissionsUnits in Hospitals With Intermediate Care Unit292readmissions
Number of ICU ReadmissionsUnits in Hospitals Without Intermediate Care Unit40readmissions

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDUnits in Hospitals With Intermediate Care Unit5,031
Overall StudySTARTEDUnits in Hospitals Without Intermediate Care Unit803
Overall StudyCOMPLETEDUnits in Hospitals With Intermediate Care Unit5,031
Overall StudyCOMPLETEDUnits in Hospitals Without Intermediate Care Unit803
Overall StudyNOT COMPLETEDUnits in Hospitals With Intermediate Care Unit0
Overall StudyNOT COMPLETEDUnits in Hospitals Without Intermediate Care Unit0

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityAdverse Events Not Collected
Total, other adverse eventsAdverse Events Not Collected00
Total, serious adverse eventsAdverse Events Not Collected00

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
25664865RESULTPubMed
28376908DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Units in Hospitals With Intermediate Care Unit vs Units in Hospitals Without Intermediate Care Unit: Vital Status at Hospital Discharge

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01422070

GET https://conductscience.org/api/trials/v1/NCT01422070/registered