Intra Hospital Mortality Risk Factors in Patients Admitted to Cardiac Intensive Care Units in 2017 in France
USIC -BNAT
1 other identifier
observational
200,000
1 country
1
Brief Summary
Retrospective, observational cohort study. Objectives: To identify intra hospital mortality risk factors in patients admitted admitted to cardiac intensive care units (CICU). The clinical main endpoint will be the observed percentage of deaths that occured during the year 2017 in french CICU. To identify the length of stay key determiners of patients admitted in french CICU. The study will use data from one of the french nationwide healthcare systems database (SNDS) : the national hospital discharge database (PMSI) to be precise.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2019
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 24, 2019
CompletedStudy Start
First participant enrolled
January 24, 2019
CompletedFirst Posted
Study publicly available on registry
February 8, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2020
CompletedAugust 11, 2022
August 1, 2022
1.9 years
January 24, 2019
August 10, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Mortality rate
Observed percentage of deaths that occured during the year 2017 in french CICU
1 day
Secondary Outcomes (1)
Length of stay at a CICU
1 year
Eligibility Criteria
Patients admitted (at least one time) in a french CICU in 2017
You may qualify if:
- Being admitted at least one time in a french CICU in 2017
- Being covered by the mandatory french national health insurance plan in 2017 without discontinuity
You may not qualify if:
- Being older than 18 years of age
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Uhmontpellier
Montpellier, 34295, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
François Roubille, MD, PhD
University Hospital, Montpellier
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 24, 2019
First Posted
February 8, 2019
Study Start
January 24, 2019
Primary Completion
December 1, 2020
Study Completion
December 30, 2020
Last Updated
August 11, 2022
Record last verified: 2022-08