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

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University of Oxford

Status

Enrolling

Conditions

Atrial Flutter
Stroke
Critical Illness
Myocardial Infarction
Atrium; Fibrillation

Treatments

Other: Admission to ICU

Study type

Observational

Funder types

Other

Identifiers

NCT04545437
PID14762
Confidentiality Advisory Group (Other Identifier)
Oxford Rec C (Other Identifier)

Details and patient eligibility

About

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.

Full 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 .

Enrollment

80,000 estimated patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

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

Trial design

80,000 participants in 1 patient group

ICU
Description:
Patients treated on a general adult intensive care unit
Treatment:
Other: Admission to ICU

Trial contacts and locations

3

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Central trial contact

Jonathan Bedford; Robert Hatch

Data sourced from clinicaltrials.gov

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