Skip to main content
Clinical Trials/NCT04545437
NCT04545437
Recruiting
Not Applicable

The Short and Long-term Cardiovascular Consequences of Critical Illness: The C3 Study

University of Oxford3 sites in 1 country80,000 target enrollmentAugust 10, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Critical Illness
Sponsor
University of Oxford
Enrollment
80000
Locations
3
Primary Endpoint
Mortality
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The aim this study will be to find out which patients are at risk of heart attacks/strokes up to several years after discharge from an ICU. This study will also investigate whether treatments and events occurring in ICU contribute to this risk.

Detailed Description

Undertake a retrospective observational cohort study of patients admitted to intensive care units between 2006 and 2023. Study Participants: Adult patients admitted to a general adult intensive care unit at one or more of the study sites between 2006 and 1st of August 2023. Objectives: To determine the short and long-term cardiovascular consequences of critical illness and identify in-ICU factors that affect them. To identify the risk factors for new-onset atrial fibrillation/flutter occurring during critical illness. To study the association between poor cardiovascular function during critical illness and long-term cardiovascular disease. This study will provide new knowledge about the associations between baseline cardiovascular risk, the disease resulting in ICU admission and therapies / events on ICU with subsequent major adverse cardiac events (MACE), to allow the ongoing risk of these events to be determined. If clinicans can idetnify who is at risk, then risk factors can potentially be modified .

Registry
clinicaltrials.gov
Start Date
August 10, 2020
End Date
December 31, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Aged 16 years or above.
  • Admitted to an intensive care unit at a study site from 2006 onwards

Exclusion Criteria

  • Patients that have informed their participating site that they do not wish their electronic records would be used for future research
  • Patients who inform us directly that they don't wish their records used in this research study

Outcomes

Primary Outcomes

Mortality

Time Frame: 5 years

Major adverse cardiovascular and vascular events

Time Frame: 5 years

Arrhythmia

Time Frame: 5 years

Secondary Outcomes

  • Hospital re-admission(5 years)

Study Sites (3)

Loading locations...

Similar Trials