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NCT06234709 Clinical Trial

Long-term Mortality After Intensive Care Considering Comorbidity and Admission Diagnoses

Critical Care Clinical Trial

Official title:
Comorbidity With Greatest Impact on Mortality Considering Different Admission Diagnosis and After Landmark Time in an Intensive Care Population Compared to the General Population

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06234709
Other study ID # Anna Aronsson Dannewitz
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2005
Est. completion date December 31, 2016

Study information
Verified date February 2024
Source Uppsala University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a register-based study The aim of this study is to investigate how common comorbidity is in different age groups and which comorbidity that has the greatest impact on mortality considering different admission diagnosis and after the acute phase compared to the general population. Also, how different degrees of comorbidity affect mortality, adjusted for other comorbidities and SAPS 3?

Description:

The study population included all patients > 16 years old admitted to an ICU during the years 2006 to 2012 and registered in the Swedish Intensive Care Registry (SIR). Hospital discharge diagnoses from in-patient care five years preceding the index time for the ICU admission were extracted from the National Patient Register (NPR) and linked to ICU admissions using unique person identity numbers. Follow-up for all-cause mortality were extracted from the cause of death register at NPR.

Recruitment information / eligibility
Status Completed
Enrollment 200000
Est. completion date December 31, 2016
Est. primary completion date December 31, 2016
Accepts healthy volunteers No
Gender All
Age group 16 Years and older
Eligibility Inclusion Criteria: The study population included all patients > 16 years old admitted to an ICU during the years 2006 to 2012 and registered in the Swedish Intensive Care Registry (SIR) Exclusion Criteria: -

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden Uppsala university department of surgical sciences Uppsala

Sponsors (2)
Lead Sponsor Collaborator
Anna Aronsson Uppsala University

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary All-cause mortality Extracted from the cause of death register at National Patient Registry in Sweden. january 1, 2005 til december 31, 2016
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