Intensive care unit outcome study

Not Applicable

Completed

• Conditions: Patients admitted to intensive care units; Not Applicable

• Registration Number: ISRCTN69112866
• Lead Sponsor: Oxford Radcliffe Hospitals NHS Trust (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2006-05-02
• Last Update Posted: 24 April 2017

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 4000

Inclusion Criteria

1. All patients that survive to discharge from a participating ICU and remained on the ICU for greater than 24 hours
2. Patients aged 16 years or older on date of ICU admission

Exclusion Criteria

1. Patients in non-participating ICUs
2. Patients admitted to a participating ICU who stayed less than 24 hours
3. Patients that do not survive to ICU discharge
4. Patients who are under 16 years old on date of ICU admission
5. Patients readmitted to an ICU and already entered in the ICON study will not have their new admission recorded

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To start and maintain a register of patients discharged from hospital after being treated for greater than 24 hours in a participating ICU.

Secondary Outcome Measures

Name	Time	Method
To evaluate in survivors of intensive care treatment:<br>1. Health-related quality of life<br>2. Risk of post-traumatic stress disorder (PTSD)<br>3. Major depression and anxiety incidence<br>4. Quality-adjusted life-years (QALYs)