Intensive Care Outcome Network Study - Phase 3

Not Applicable

Completed

• Conditions: Former intensive care patients of participating hospitals; Not Applicable

• Registration Number: ISRCTN88066041
• Lead Sponsor: niversity of Oxford (UK)

Brief Summary

1. 2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/30466485

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-08-01
• Study Completion: 2014-05-31
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 1000

Inclusion Criteria

1. Aged at least 16 years on admission to intensive care
2. Participants must have experienced at least 24 hours of level three dependency care (ICU care) at any time during their hospital stay and survived until the time of hospital discharge

Exclusion Criteria

1. Aged under 16 years
2. Unable to complete questionnaires and have no consultee to fill in the forms on their behalf
3. Foreign nationals
4. In residential care
5. In prison
6. Unwilling to consent
7. Life status cannot be traced (i.e. have no GP or NHS numbers)

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Data from the ICON study will allow the identification of risk factors for poor long-term outcomes after patients have been treated on an intensive care unit, which will in turn inform the development of effective treatments and enable earlier recognition of factors related to poor long-term outcome in these patients. This entire process has the ultimate goal of improving the long-term quality of life of patients who have experienced treatment on an intensive care unit.