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Intensive care unit outcome study

Intensive care unit outcome study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN69112866
Enrollment
4000
Registered
2006-05-02
Start date
2006-03-01
Completion date
Unknown
Last updated
2017-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients admitted to intensive care units Not Applicable

Interventions

Questionnaires regarding health-related quality of life (HRQOL).

Sponsors

Oxford Radcliffe Hospitals NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

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

Secondary

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

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 5, 2026